Multipoint source method in air pollution modelling of cold start emission

The paper presents a new method of air pollution modelling on a micro scale. For estimation of concentration of car exhaust pollutants, each car is treated as an instantaneous moving emission source. This approach enables us to model time and spatial changes of emission, especially during cold and cool start of an engine. These stages of engine work are a source of significant pollution concentration in urban areas. In this work, two models are proposed: one for the estimation of emission after cold start of the engine and another for the prediction of pollutant concentration. The first model (defined for individual exhaust gas pollutants) enables us to calculate the emission as a function of time after the cold or cool start, ambient temperature and average speed of motion. This model uses the HBEFA database. The second mathematical model is developed in order to calculate the pollutant dispersion and concentrations. The finite volume method is applied to discretise the set of partial differential equations describing wind flow and pollutant dispersion in the domain considered. Models presented in this paper can be called short-term models on a small spatial scale. The results of numerical simulation of pollutant emission and dispersion are also presented.     

过硫酸钾氧化-紫外光度法测定总氮方法的改进

过硫酸钾氧化紫外光度法测定总氮的空白吸光度高的主要原因是：K2S2O3是220nm波长上有特征吸收，适当降低K2S2O3、NaOH的用量，延长消解时间，使用二次蒸馏水，用低浓度亚砷酸钠溶液，还原消解后剩余的极少量的K2S2O3，可以降低空白吸光度。K2S2O3-NaOH碱溶液不稳定，使用期短，三天后氧化能力迅速降低，原因是：K2S2O3溶液中，加入NaOH，加速了K2S2O3的分解。K2S2O3和NaOH分别配制，并在K2S2O3溶液中，加入少量HCl，抑制其水解。两种溶液可使用半年以上时间。     

Determination of arsenic in grain and soil by hydride nondispersive atomic fluorescence method

Quantity of trace arsenic in grain and soil was determined by hydride nondispersive atomic fluorescence method.Optimum conditions of measurement were selected in the experiment including the pH of the medium, reductive agent, the concentration and flowing velocity of KBH4, rate of carrier gas and atomized temperature. The reference sample of rice C was determined and the linear relationship of the calibration curve was plotted, indicating that the method was highly precise. In the experiment of recovery rate, the method was quite satisfactory.Based on the determination of hundreds of samples, it is proved that atomic fluorescence method is rapid, sensitive and low in interference. It is very efficient on determination of trace arsenic in soils and grains, especially in grains.     

恶臭污染防治技术及工程实践

目前，恶臭污染对人类生活的危害日益加剧，文中介绍了几种恶臭污染物的防治技术。对生物滴滤池 活性炭吸附工艺进行了探讨，工程实例表明具有良好的治理效果。     

钢门框型材冷弯成形工艺

介绍了不对称钢门框型材孔型设计中工艺参数、变形方式的选择方法     

火焰原子吸收分光光度法测定水中锶

研究了用空气/乙炔火焰原子吸收分光光度法测定水中锶时酸的影响,以及铝和钙的干扰及消除,线性范围0.05～5.00mg/l,最低检测浓度为0.04mg/l,回收率为98.2％～101.4％。     

微波消解-原子荧光法测定海洋沉积物中As的研究

研究了微波消解海洋沉积物中的As,在比较几种不同的酸消解体系后,得到适合海洋沉积物分析的酸消解体系.与传统的湿法消解比较,测试结果无显著性差异.微波消解具有快速高效、试剂用量少、空白值低、样品不易挥发等优点,已成为海洋沉积物样品前处理的有效手段.     

Quantitative structure-property relationship of aromatic sulfur-containing carboxylates

IntroductionItiswidelyrecognizedthatthephysicochemicalprofileoforganicchemicalslargelydeterminestheirdistributionbetweenenvironmentalmedia .Fortheenvironmentalbehaviorsoforganiccontaminants,watersolubility(SW)andoctanol waterpartitioncoefficient(KOW)aretremendouslyimportant.Octanol waterpartitioncoefficienthasbeenwidelyrelatedtobiochemicaland orbiologicalactivityinquantitativestructure activityrelationships(QSARs) (Leo ,1 971 ) .Watersolubilitycorrespondstothedispersiontendencyandtothereca…     

Quantification of human amniotic fluid constituents by high resolution proton nuclear magnetic resonance (NMR) spectroscopy

We have investigated the ability of high-resolution proton NMR spectroscopy to provide a biochemical constituent screening of human amniotic fluid (AF). Proton NMR spectra were obtained at 300 MHz on AF from patients undergoing amniocentesis in the mid-trimester. Only AF from normal pregnancies (normal fetal karyotype, normal a-fetoprotein levels, normal birth outcome) was used in this study. The AF supernatant was lyophilized and resuspended in deuterated water containing 0.1 mm phosphate buffer and 6.02 mm disodium maleate. Identification of low molecular weight compounds was confirmed by two-dimensional NMR spectra (primarily correlated spectroscopy, or COSY) and standard addition techniques. A broad profile of compounds were ‘NMR visible’ in a single proton spectrum, including creatinine, glucose, organic acids (acetate, citrate, and lactate) and several amino acids (alanine, histidine, leucine, phenylalanine, tyrosine and valine). The proton spectrum was unaffected by prior freezing/thawing of AF samples. We were able to quantify compounds by comparison with an added concentration standard (maleate) at concentrations as low as 30 μm. Good agreement with literature values based on other analytical techniques was obtained.     

在磁场中活性炭吸附有机物的研究

将磁化技术引入吸附过程中，考察了磁场处理对活性炭吸附苯、硝基苯、苯甲酸、氯苯和苯酚的影响．结果表明，预磁处理能使非极性物质苯和极性较小的氯苯、苯酚在活性炭上的吸附容量减小，而使极性较大的苯甲酸和有NO2基团的硝基苯的吸附容量增大．增大磁场强度能加强苯和苯甲酸的磁处理效果。