镉─邻菲啰啉配合物吸附波的研究与应用

在ｐＨ３．３的盐酸－醋酸钠介质中．镉－邻菲啉配合物在－０．６５Ｖ（ｖＳ．ＳＣＥ）处产生一灵敏的吸附波，其二次导数波高与镉浓度在０．０００６～０．１ｍｇ／Ｌ范围内呈良好的线性关系，检出下限达０．０００３ｍｇ／Ｌ。极谱波性质的研究表明该波具有配合物吸附波的特征。方法已用于环境水样中微量错的测定，结果与其它方法吻合。     

水环境数学模型在河流水质管理规划中的应用

本文讨论了水环境数学模型的选择及在水质管理规划中的使用方法,达到实用的目的.具有广泛的通用性和实用性.     

Evaluation of interference to conventional and real-time PCR for detection and quantification of fungi in dust

Advances in polymerase chain reaction (PCR) have permitted accurate, rapid and quantitative identification of microorganisms in pure cultures regardless of viability or culturability. In this study, a simple sample processing method was investigated for rapid identification and quantification of fungal spores from dust samples using both conventional and real-time PCR. The proposed method was evaluated for susceptibility to interference from environmental dust samples. Stachybotrys chartarum and Aspergillus fumigatus were used as test organisms. The sensitivity of detection in pure culture was 0.1 spore DNA equivalents per PCR reaction corresponding to 20 spores ml(-1) in the sample. However, 1 spore DNA equivalent per PCR reaction corresponding to 200 spores ml(-1) in the sample was the lowest amount of spores tested without interference in dust samples spiked with spores of either fungal species. The extent of inhibition was calculated using conventional and real-time PCR reactions containing fungal spores, specific primers, specific probes (for real-time PCR) and various amounts of dust. The results indicate that the extent of inhibition by dust on PCR varies with the type and amount of dust, and number of spores. No interference in the analysis of spiked samples was detected from 0.2 mg ml(-1) of four real-life dust samples at p-value >0.05 using 2 x 10(4) spores for conventional PCR and 2 x 10(5) spores for real-time PCR. However, samples containing >0.2 mg ml(-1) real-life dust compromised the PCR assay. These results suggest the potential usefulness of a simple sample processing method in conjunction with PCR for monitoring the fungal content of aerosols collected from indoor environments.     

基于N，N─二甲基苯胺与NO_2~－─对氨基苯磺酸重氮盐的偶联反应示波极谱法测定NO_2~－

报道了利用Ｎ，Ｎ─二甲基苯胺为偶联试剂的Ｃｒｉｅｓｓ反应以示波极谱法测定ＮＯ_２~－的测试方法。在拟定的实验条件下，ＮＯ_２~－在４．０×１０~－３～４．８×１０~－１μｇ／ｍｌ范围内与极谱波波高呈良好的线性关系。环境水测定的相对标准偏差小于ｌ％，回收率在９７％～１０１％之间。     

中国土壤中溴,碘的背景含量

通过对全国八百余个表层土样的分析测试,获得了中国土壤中溴、碘背景含量的总体水平及在各土类中的含量,相对于地壳丰度,中国土壤中溴、碘普遍得到了富集,溴、碘含量分异变化较大,并具有明显的地域分异特征,影响中国土壤中溴、碘含量的主要因素是降水量、土壤吸附体的含量以及某些特殊母质。     

密切值法在污染源治理方案优选中的应用

本文采用密切值法进行污染源多个治理方案的优化决策研究，并通过实例分析获得了与实际状况相符合的优化结果。     

用液相催化法和脱硫除尘器脱除烟气中SO_2

在由旋风水膜和两块旋流塔板组成的处理气量为７５０ｍ￣３／ｈ的二级脱硫除尘器中，进行了用含催化剂Ｍｎ￣（２＋）的水溶液吸收ＳＯ_２的扩大试验。结果表明，在确定的条件下，脱硫率达到７３％，板效率为０．２５～０．２８。在同一设备中同时完成除尘与脱硫过程，设备投资少；以水为吸收剂，运行费用低；中性条件下吸收，长期运转不结垢，可靠性高。     

中国黄土元素背景值分异规律研究

报道了中国黄土中40个元素的背景值,并以F、Cr、Mn、Co、Ni、V、Cu、Zn、As、Se、Cd、Pb、Hg等13个元素为例,讨论了其在黄土高原的分布与含量。利用趋势面分析等数理统计方法,揭示了黄土中元素的某些环境地球化学特征及元素背景值的分异规律。结果表明,黄土的元素背景值具有三维的分异特征,黄土的质地及沉积的生物气候环境黄土是影响背景值分异的主要因素。为中国黄土的风成学说提供了佐证。     

Heavy metals in water bodies purified by suspended substrate of rivers

ＩｎｔｒｏｄｕｃｔｉｏｎＨｅａｖｙｍｅｔａｌｓｉｎｗａｔｅｒｂｏｄｉｅｓａｒｅｓｉｇｎｉｆｉｃａｎｔｌｙｄｉｆｆｅｒｅｎｔｆｒｏｍｏｒｇａｎｉｃｐｏｌｌｕｔａｎｔｓｔｈａｔｃａｎｂｅｍｉｃｒｏｂｉｏｌｏｇｉｃａｌｌｙｄｅｇｒａｄｅｄｏｒｄｅｃｏｍｐｏｓｅｄ .Ｇｅｎｅｒａｌｌｙ ,ｔｈｅｙａｒｅｐｕｒｉｆｉｅｄｔｈｒｏｕｇｈｔｈｅｉｒａｄｓｏｒｐｔｉｏｎｏｎｔｏｓｕｓｐｅｎｄｅｄｓｕｂｓｔｒａｔｅｓｉｎｒｉｖｅｒｓ.Ａｄｓｏｒｐｔｉｏｎｏｆｈｅａｖｙｍｅｔａｌｓｏｎｒｉｖｅｒｓｕｓｐｅｎｄｅｄｓｕｂ…     

GHG emission reductions and costs to achieve Kyoto target

Emission projection and marginal abatement cost curves (MACs) are the central components of any assessment of future carbonmarket, such as CDM (clean development mechanism) potentials, carbon quota price etc. However, they are products of very complex,dynamic systems driven by forces like population growth, economic development, resource endowments, technology progress and so on. The modeling approaches for emission projection and MACs evaluation were summarized, and some major models and their results were compared.Accordingly, reduction and cost requirements to achieve the Kyoto target were estimated. It is concluded that Annex I Parties‘ total reduction requirements range from 503--1304 MtC with USA participation and decrease significantly to 140--612 MtC after USA‘ s withdrawal. Total costs vary from 21--77 BUSD with USA and from 5--36 BUSD without USA if only domestic reduction actions are taken. The costs would sharply reduce while considering the three flexible mechanisms defined in the Kyoto Protocol with domestic actions‘ share in the all mitigation strategies drons to only 0--16%.