Transportation and fate of cationic surfactant in river water

The degradation, sorption, transportation and material balance of cationic surfactants discharged from domestic waste into river water was studied. Ion-pair solid-phase extraction behavior showed that the sorption of cationic surfactants as an ion-pair with anionic surfactant onto river sediment was so strong that little cationic surfactant was found in the bulk water. Cationic surfactant was found in river sediment at more than 500 times higher concentration than that in the bulk water. The degradation of the cationic surfactant was very slow in river water and much slower in the sediment. A material balance of cationic surfactant was estimated for a river running through Toyama City by measuring the flow rate and the concentration of cationic surfactant in the water at several points. It was found that more than 30% of cationic surfactant introduced to the river was lost during the river running through ca. 3 km in 3 h. This reduction probably comes from a quick transfer of the cationic surfactant from river water to sediment and water weed by means of adsorption or precipitation with suspending solids.     

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。     

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。     

连续化学浸提法测定底泥中不同形态汞的探讨

本文提出用连续化学浸提法将底泥作连续五次抽提,根据不同形态汞的溶解度,将底泥中汞分为水溶性汞、酸溶性汞、碱溶性汞、硝酸溶汞、王水溶汞五个部分。对蓟运河沿岸的天化、茶淀和污水库底泥中汞作上述化学形态分析。用合成样品验证求回收率,认为对底泥中惰性汞的测定较热解法可靠,并发现底泥中腐殖质汞与惰性汞之间有相关关系。     

Heavy metals in water bodies purified by suspended substrate of rivers

ＩｎｔｒｏｄｕｃｔｉｏｎＨｅａｖｙｍｅｔａｌｓｉｎｗａｔｅｒｂｏｄｉｅｓａｒｅｓｉｇｎｉｆｉｃａｎｔｌｙｄｉｆｆｅｒｅｎｔｆｒｏｍｏｒｇａｎｉｃｐｏｌｌｕｔａｎｔｓｔｈａｔｃａｎｂｅｍｉｃｒｏｂｉｏｌｏｇｉｃａｌｌｙｄｅｇｒａｄｅｄｏｒｄｅｃｏｍｐｏｓｅｄ .Ｇｅｎｅｒａｌｌｙ ,ｔｈｅｙａｒｅｐｕｒｉｆｉｅｄｔｈｒｏｕｇｈｔｈｅｉｒａｄｓｏｒｐｔｉｏｎｏｎｔｏｓｕｓｐｅｎｄｅｄｓｕｂｓｔｒａｔｅｓｉｎｒｉｖｅｒｓ.Ａｄｓｏｒｐｔｉｏｎｏｆｈｅａｖｙｍｅｔａｌｓｏｎｒｉｖｅｒｓｕｓｐｅｎｄｅｄｓｕｂ…     

环境科学研究中两变量非线性相关时的线性回归方程

以环境科学研究两变量非线性相关的问题为对象，讨论建立线性回归方程的方法。有绝对误差均方和最小的最小二乘法、相对误差最小的新回归法。以简易的方法，建立相关性好、误差小的回归方程。介绍了两变量各种非线性相关时的线性回归方程在环境科学研究中的应用。     

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%.