微波消解-电感耦合等离子体质谱法测定铁矿石中铬砷镉汞铅

铁矿石中Cr、As、Cd、Hg和Pb不仅影响冶炼设备和产品性能,同时污染环境。文章以铁矿石标准物质为研究对象,对电感耦合等离子体质谱法(ICP-MS)测定铁矿石中Cd、As、Cr、Hg和Pb等5种元素进行了适用性探讨。结果表明,与常规的单元素原子吸收光谱法或多元素同步分析电感耦合等离子体发射光谱法相比,用微波消解方法处理铁矿石,具有样品消耗量少(0.1000±0.0200)g、消解用酸少(2.5 mL HCl+0.5 mL HF+1.0 mL HNO3)、排放降低、节约成本等优点,且无需配制铁底液,无需添加任何掩蔽剂,质谱干扰小,适用于分析Cr含量为5.5×10-10～2.5×10-4,As含量为7.6×10-10～1.9×10-4,Cd含量为4.5×10-11～5.5×10-6,Hg含量为1.88×10-9～1.9×10-7,Pb含量为1.2×10-10～3.2×10-5的铁矿石样品。优化后的前处理方法节约了能源、试剂和样品消耗,降低了二次污染和有效损失。     

内蒙古巴丹吉林沙漠400年来大气沉降 Hg的湖泊沉积记录

Hg污染具有全球性,人类活动较少地区的湖泊沉积物对长距离输入的大气沉降Hg变化敏感。巴丹吉林沙漠中发育了约142个沙漠丘间湖泊,是研究大气沉降Hg记 录的理想材料。选择巴丹吉林沙漠东南部的宝日陶勒盖湖泊进行湖泊钻探,结合²¹⁰Pb_uns和¹³⁷Cs核素测年及THg沉积通量计算,重建了400年来巴丹吉林沙漠湖泊的THg沉积记录,并探讨了影响沙漠湖泊THg沉积的影响因素,评估了自然背景和人类活动的影响。结果表明：(1)沉积物中THg含量分布范围为1.5~17.5 ng/g,富集系数和沉积通量的分布范围分别为0.3~4.5和2.9~38.9 μg/(cm²·a)。 THg含量、富集系数和沉积通量均表现为在岩心上部近几十年富集。(2)近400年来,湖泊沉积物中背景THg(THg_岩石风化)通量变化相对稳定,主要受控于附近物源供给和区域风沙活动。大气沉降THg(THg _大气)通量自20世纪30年代以来呈逐渐增加的趋势,很大程度上反映了近几十年来人为源大气沉降THg的增加。但20世纪30年代以来岩心局部的大气沉降THg通量的峰值可能还受全球变暖和湖泊生产力增加 的影响,而20世纪30年代之前出现的峰值可能与“小冰期”冷期强烈的区域风沙活动有关。巴丹吉林沙漠湖泊400年来的THg_大气沉积通量变化与全球Hg产量和冰心中的大气Hg含量变化记录一致,是沙漠 地区大气沉降THg的可信纪录。     

Variations of levels and composition of PM10 and PM2.5 at an insular site in the Western Mediterranean

The insular suburban site of Castillo de Bellver was selected for the study of the variability of PM levels and composition in the Western Mediterranean Basin (WMB).Mean annual (in 2004) PM₁₀ and PM_2.5 levels at this site were 29 and 20 µg/m³, respectively. These levels may be regarded as relatively low when compared with other suburban insular locations in the Eastern Mediterranean Basin (EMB), but they are higher than those recorded at most of the European suburban sites, especially in Northern and Western Europe. Seasonal variability of PM levels at this site is governed by meteorology rather than local emissions, whereas the daily cycles are clearly defined by the anthropogenic emissions, mainly coming from the urban area of Palma de Mallorca and the harbour area of the same city.Concerning the aerosol composition at this site, the main PM constituent is the mineral matter (29% in PM₁₀ and 16 % in PM_2.5), more than 50% (in PM₁₀) being attributable to African dust. The amount of secondary inorganic aerosols is also very high (27% in PM₁₀ and 34% in PM_2.5), with the predominance of fine ammonium sulphate, and in a less proportion fine ammonium nitrate (in winter) and coarse Ca and Na nitrate (with higher importance in summer). The carbonaceous particles, dominantly fine, account for 17% of PM₁₀ and 25% of PM_2.5. The elemental carbon/organic carbon (EC/OC) ratio reached a mean value of 0.17, similar to those observed at regional background sites in the WMB coast of Spain. The sea spray aerosols (mainly coarse) represented around 10% of PM₁₀, and only 4% in PM_2.5. Finally, the unaccounted fraction increased from 15% to 20% in PM_2.5, being mostly attributed to water.The concentrations of trace elements in PM₁₀ and PM_2.5 were usually in the range to those observed in regional background sites in the Iberian Peninsula, with the exception of the typical tracers of road traffic such as Cu, Sb, Zn, Sn and Ba, which presented concentrations in the range of urban sites of Iberia. Other elements such as Cr, Zr, Hf and Co have been identified as the main tracers of the harbour contributions.     

贵州滥木厂汞矿区土壤与大气间气态汞交换通量及影响因素研究

利用动力学通量箱-大气自动测汞仪联用技术,分别于2002年12月和2003年5月对贵州省西南部滥木厂汞矿区5个采样点的土壤汞释放通量进行了系统的测定.结果表明该区土壤是大气的重要汞释放源.5个采样点土壤释汞通量最高值达10 543.7 ng/(m2·h),平均值最高达(2 283.3±2 434.2)ng/(m2·h)(n=152).结果显示土壤总汞含量与土壤释汞通量关系密切,是决定土壤汞释放的内在因素,光照、温度、湿度和大气汞含量等环境因素与土壤释汞通量有较好的相关性,对土壤汞的释放有显著的影响.     

滇黔桂地区汞锑金砷等低温矿床组合碳,氢,氧,硫同位素地球化学

滇黔桂地区分布着众多大中型Hg、Sb、Au矿床。通过对碳、氢、氧、硫等同位素的分析表明：大厂锑矿的硫来自地幔，木利、马雄锑矿的硫主要来自海水硫酸盐。各金矿的硫主要来自围岩，但碳大部分来自围岩。氢氧同位素数据表明，本区锑、金、汞等矿床的成矿流体来源相似，其主要来源为与围岩进行了氢氧同位素交换的大气降水。     

Export fluxes of biogenic matter in the presence and absence of seasonal sea ice cover in the Chukchi Sea

Drifting sediment traps were deployed at 9 stations in May-June (ice-covered conditions) and July-August (ice-free conditions) 2004 in the Chukchi Sea to investigate the variability in export fluxes of biogenic matter in the presence and absence of sea ice cover. Measurements of chlorophyll-a (Chl-a), particulate organic carbon (POC), particulate nitrogen (PN), phytoplankton, zooplankton fecal pellets, and the stable carbon isotope composition (δ¹³C) of the sinking material were performed along Barrow Canyon (BC) and a parallel shelf-to-basin transect from East Hanna Shoal (EHS) to the Canada Basin. POC export fluxes were similarly high in the presence (378±106 mg C m⁻² d⁻¹) and in the absence of ice cover (442±203 mg C m⁻² d⁻¹) at the BC stations, while fluxes were significantly higher in the absence (129±98 mg C m⁻² d⁻¹) than in the presence of ice cover (44±29 mg C m⁻² d⁻¹) at the EHS stations. The C/N ratios and δ¹³C values of sinking organic particles indicated that POC export fluxes on the Chukchi continental shelf were mostly composed of freshly produced labile material, except at the EHS stations under ice cover where the exported matter was mostly composed of refractory material probably advected into the EHS region. Chl-a fluxes were higher under ice cover than in ice-free water, however, relatively low daily loss rates of Chl-a and similar phytoplankton carbon fluxes in ice-covered and ice-free water suggest the retention of phytoplankton in the upper water column. An increase in fecal pellet carbon fluxes in ice-free water reflected higher grazing pressure in the absence of ice cover. Elevated daily loss rates of POC at the BC stations confirmed other indications that Barrow Canyon is an important area of carbon export to the basin and/or benthos. These results support the conclusion that there are large spatial and temporal variations in export fluxes of biogenic matter on the Chukchi continental shelf, although export fluxes may be similar in the presence and in the absence of ice cover in highly productive regions.     

天然磁铁矿处理含Hg（Ⅱ）废水实验研究

利用重金属离子可在水合金属氧化物和氢氧化物矿物表面产生吸陵作用的原理，进行了天然磁铁矿处理含Hg(Ⅱ）废水的实验研究，结果表明：当温度为25℃，吸附平衡时间为60分钟、试样用量为20g/L，试样粒径为200目以下、pH值为6.40，离子强度为零时，Hg(Ⅱ）初始浓度为1.12mg/L的溶液的吸附率可达98%，使废水中Hg(Ⅱ）的浓度达到国家排放标准。pH值、离子强度、粒径、试样用量、废水浓度、温度、时间均对Hg(Ⅱ）的吸附率有一定的影响，其中pH值的影响最大，Hg(Ⅱ）在天然磁铁矿上的吸附等温曲线不同于Langmuir和Freundlich等温曲线，而是表现为台阶段，符合分级离子/配位子交换等温曲线。     

Seasonal and event-controlled export of organic matter from the shelf towards the Gulf of Lions continental slope

To investigate the role of coastal canyons in the transfer of organic matter from the shelf to the slope and basin, we deployed sediment trap/current meter pairs at the head of five canyons in the Gulf of Lions (GoL) between November 2003 and May 2004. Analysis of organic carbon, biogenic silica, Corg isotopic composition, Corg/total nitrogen, chloropigments, and amino acids clearly shows the seasonal influence and effect of extreme meteorological events on the composition of collected particles. The sampling period was divided into three “scenarios”. The first corresponded to a large easterly storm and flood of the Rhone river during stratified water column conditions; the composition of material collected during this event was influenced by increased transfer of riverine and coastal particulate matter, with a lower Corg content. During the second “fall-winter” scenario, northern and northwestern winds blowing over the shelf caused cooling and homogenization of the shelf water column; particles collected at this time reflected the homogeneous source of particulate matter transported through canyons; particles sitting in the vicinity of canyon heads are most likely swept downslope by the general south-westward circulation. Organic tracers indicate a degraded origin for organic matter transported during this period. A third “spring” scenario corresponded to northern winds alternating with eastward windstorms that triggered and/or enhanced the cascading of dense waters accumulated on the bottom of the shelf due to previous cooling. These conditions occurred in conjunction with increased phytoplankton productivity in shelf surface waters. Organic matter advected mainly by dense shelf water cascading was fresher due to the transport of newly produced particles and a variable terrestrial fraction; this fraction depended on the proportion of resuspended material accumulated during previous high discharge periods that was involved in each transport pulse. The tight link shown between meteorological conditions and organic matter transport is important for continental margin geochemical studies as future changes in climatic conditions may lead to dramatic changes in carbon sequestration capability and in the ecosystems of deep margin environments.     

云南富源—弥勒1∶5万化探异常的发现及意义

1∶5万水系沉积物测量表明,该区属浅成低温热液型金多金属成矿区,除受构造控制外,岩浆岩、地层亦有控矿作用。金矿主要分布在裂谷带中,成矿潜力巨大,测区西部杨梅山中部支壁找铜金、东南部大得克找铅锌有较好前景。     

The degree of Cl-loss for the particulate matter (PM) and fog water sampled at the same air mass at the Hachimantai mountain range in northern Japan

It is well known that sea-salt aerosols in particulate matter (PM) react with acids such as H₂SO₄ and HNO₃ during transportation and thereby lose chloride ions (Cl-loss). The PM and fog were sampled concurrently at different altitudes in the Hachimantai mountain range, northern Japan. The PM and fog sampled at different altitudes had nearly identical properties for the ion components. However, the PM was in a Cl-depleted state (more than 80% of all samples), but the fog water was not in so Cl-depleted state (less than 29%). As a result, it could be explained that this phenomenon caused because the fog droplets took up the gaseous state HCl other than sea-salt PM. After all Cl^- in the fog water recovered and was rather rich compared with the sea-salt or the PM by the uptake of the gaseous state HCl. Moreover, it was found that for PM_coarse(2.5 < D < 10), 86% of the acid (H₂SO₄ and HNO₃) was consumed for Cl-loss reactions and/or for dissolution of Ca and Mg in soil particles.