排出障碍，开发生物质气化技术

生物质气化是把废物转化气体,它对开创新兴可再生能源来源是有潜力的,但须避免工厂产生不必要的副产品,另外还要找到可靠且稳定的生物质来源,但这并非易事。     

北京市土壤Hg污染的区域生态地球化学评价

城市土壤Hg异常/污染是中国普遍存在的重大生态环境问题。文章对北京市近1000km2范围内的地表土壤、壤中气、大气干湿沉降、大气颗粒物、大气中的Hg含量水平和空间分布模式进行了系统研究,查明北京地表土壤Hg平均含量为0.41mg/kg,大气干湿沉降物中的Hg平均含量为0.194mg/kg,壤中气Hg的平均含量为559.65ng/m3,大气颗粒物PM10和PM2.5中的Hg含量分别为0.59和0.67ng/m3,大气中的Hg平均含量为3.13ng/m3。北京市自2000年起实现了由燃煤转变为燃气的减排措施,导致干湿沉降物中的Hg沉降通量显著减少,2006年大气干湿沉降物中Hg的沉降通量1.837mg·m-2·a-1,北京市城区(近1000km2)Hg全年沉降为1837kg,空气中总Hg浓度由1998年的8.3~24.7ng/m3下降到2006年的3.13ng/m3,大气颗粒物中Hg含量由2003年的1.18ng/m3下降到2006年的0.59ng/m3(PM10)和0.67ng/m3(PM2.5),表明北京市煤改气减排措施的实施显著改善了大气环境质量。通过对土壤中Hg的存在形式研究,发现土壤中有硫化物(辰砂)及各种Hg盐(HgCl2)的含Hg矿物,Hg也可以各种吸附方式或壤中气方式存在。研究证实北京壤中气Hg与大气Hg存在显著的相关性(n=131,R=0.267,p<0.01),表明壤中气Hg是大气Hg的重要来源之一。利用2005年地表土壤总Hg与Hg释放速率的线性方程估算,土壤Hg平均释放速率为102.42ng·m-2·h-1,2005年土壤释放进大气的Hg通量为936.70kg。在查明土壤中存在大量辰砂矿物的同时,还分布有大量具有高温熔融特征的金属微球粒和玻璃质微球粒,证明燃煤和冶金烟尘是地表土壤Hg的主要来源。土壤中Hg、S、pH和辰砂颗粒浓度在空间上的高度耦合性表明,碱性条件下,土壤中高含量的S和Hg是辰砂形成的重要原因。按国家土壤环境质量标准,北京市I级土壤Hg环境质量的面积为176km2,Ⅱ级为808km2,Ⅲ级为24km2,超Ⅲ为36km2。Ⅲ级、超Ⅲ级主要分布在二环路以内的中心城区。城南(长安街为界)大气Hg环境质量明显优于城北,在北四、北五环之间的部分地区,大气颗粒Hg的环境质量为Ⅲ级或超Ⅲ级。在地表土壤Hg含量较高的中心城区,居民每天因呼吸摄入的Hg高达364ng,对人体健康构成潜在风险。根据我国"十一五"规划中每年实现10%节能减排的目标,对北京市未来50年土壤Hg含量的时空演变趋势预测,预测2050年北京因干湿沉降带来的Hg输入量为16.03kg,地表土壤释放Hg的输出量为37.36kg,明显大于Hg的输入通量,土壤Hg的环境质量将得到根本改善。预测到2040年Ⅲ级土壤Hg环境质量的区域将完全消失,到2060年以Ⅰ级土壤为主。     

太湖秋季光学活性物质空间分布及其遥感估算模型研究

基于2004年秋季在太湖进行的一次大范围水体吸收系数、散射系数、辐照度比等生物光学特性及光学活性物质浓度的测定和计算,分析了秋季太湖光学活性物质浓度的空间分布特征以及水体生物光学特性,并在此基础上发展了内陆浅水湖泊非色素颗粒物、浮游植物色素和有色可溶性有机物(chromophoric dissolved organic matter,CDOM)的半分析模型.     

河流活性物质入海通量:概念与方法

河流水体中呈溶解态和悬浮物结合态的元素活动性强,具有生态环境意义,查明其入海通量是当前生态地球化学评价的重要任务。通过总结前人的相关研究成果,确定了影响河流水体悬浮物的浓度及其矿物、化学组成的主要因素。从沿海经济带区域生态地球化学评价的实际需要出发,拟定了开展中国主要入海河流水溶态和悬浮物结合态元素入海通量调查的基本框架。     

太原盆地农田区大气降尘对土壤重金属元素 累积的影响及其来源探讨

通过研究太原盆地大气干湿沉降中重金属元素的含量分布特征及年输入通量,讨论其对土壤中重金属元素累积的影响。同时采用富集因子法探讨降尘物质的来源。研究结果表明,降尘中重金属元素As、Cd主要来源于人为活动,Pb的来源可能是人为源和自然源。而Hg则主要来源于自然源。     

陕西关中盆地中部地下热水H、O同位素交换 及其影响因素

对关中盆地地下热水δ＆18O和8D数据的研究表明：盆地中部西安、咸阳深部的地压地热流体发生明显的δ^18O同位素交换,并出现^2H同位素交换,表明热储流体发生了强烈的水岩反应,盆地周边及中部的非地压地热流体^18O交换则不明显。根据研究区^18O同位素的交换程度（用^2H过量参数d表征）和水化学资料,可将关中盆地热储流体分为循环型和封闭型热储流体2类。地热水埋深越大、滞留时间越长、TDS和温度越高、地质环境越封闭,18^O交换程度就越大。西安和咸阳地下热水分属于不同的地热系统,具有不同的补给来源。     

锦州湾泥沙来源、洄淤状况与建港条件分析

锦州湾泥沙主要来源于沿岸入海河流的输送,外海水体的携带与沿岸、岛屿蚀余物质的补给。每年进入湾内的泥沙总量约为３３—３５万吨,假如这些泥沙不再向湾外流出,在湾内作均匀分配沉积,则相当于在湾底铺上５ｍｍ厚的土。水准和水深重复测量表明,潮滩以稳定的弱堆积为主,水下浅滩基本处于稳定状态。该湾在非正常情况下产生骤淤的可能性不大。综合建港条件良好。     

Associations and mobility of uranium in soils near a depleted uranium （DU） weapons testing site, SW Scotland

Natural uranium has three isotopes, ^238U, ^235U and ^234U, with natural abundances of 99.27 atom %, 0.72% and 0.0055%, respectively. Only ^235U is fissile and the production of nuclear fuel and nuclear weapons involves enrichment of uranium in ^235U. This process also results in separation of ^234U from ^238U, leaving depleted uranium （DU）, with typical ^234U/^238U and ^235U/^238U activity ratios of about 0.19 and 0.013, respectively, as a waste product. The high density, high melting and boiling points and chemical stability of uranium and the availability of DU in relatively pure form mean that DU has many uses, including armour-piercing munitions. Such munitions have been developed in the UK since the 1960s and testing has been carried out by the Ministry of Defence （MoD） at firing ranges such as Dundrennan, SW Scotland and Eskmeals, NW England. The firing of DU munitions can result in the dispersion of DU and its combustion products （oxides） as aerosols or as larger fragments, with the potential for human exposure either directly at the site of detonation or via post-depositional migration in the environment. The aim of this work was to investigate the potential environmental mobility of DU by characterizing the associations of U in soil porewaters with increasing distance from a firing site. To this end, several soil cores located down-wind of the firing site at Dundrennan, near Kirkcudbright, SW Scotland, were collected in May 2006. These were sectioned on-site into 1- or 2-cm depth intervals and porewaters were isolated by centfifugation （10 minutes; 8873 g） on return to the laboratory. Following filtration through 0.2-micron cellulose nitrate filters, the porewaters were analyzed by ICP-QMS （U concentration） and ICP-OES （Fe, Al, Ca, Mg, Mn concentrations）. Sub-samples were also subjected to centrifugal ultrafiltration （100, 30, and 3 kD） and to gel electrophoretic fractionation （agarose; 0.045 M Tris-borate; 20 mA, 30 minutes）. Results showed that U was present at up to 4 μg/L in the soil porewater and that the associations of U varied with sample location and soil depth.     

Water chemical behavior at Yangtze （Changjiang） River estuary

Geochemical cycling has received wide attention due to the need to understand the pathways of pollutants through our present environment. In this regard the Yangtze River plays a significant role in putting those pollutants into the East China SeafWorld Oceans. The Yangtze River is of high sedimentation rate and water discharge. The watershed covers variable climate regions from temperate to subtropical and from semiarid to humid. Twenty three （23） sampling locations at the estuary have been selected for understanding the dynamic relationships. The elements （Cl^-, SO4^2-, Na^＋, K^＋, and Ca^2＋） show conservative behavior during mixing of fresh water with saline water whereas Mg^2＋, Mn^2＋ show a non-conservative pattern . The relationships between Na^＋/SO4^2- and Cl^-/SO4^2- molar ratios show a mixing of more than two water sources.