PM10冲击采样器切割头设计参数对切割粒径的影响

本文从颗粒在气流中的受力情况分析入手 ,得到冲击采样器中喷嘴喷出后颗粒的运动轨迹方程以及运动轨迹与采样器切割头设计参数的关系式。分析了PM10空气采样器的切割原理 ,并利用数值计算研究颗粒在不同的流量、喷嘴尺寸及喷嘴与冲击板的距离下的运动轨迹 ,从而得到切割头设计参数对切割粒径的影响     

宁波-舟山海域入海污染物环境容量研究

在宁波-舟山海域数值模拟潮流场的基础上,建立了该海域各污染源的响应系数场,计算了主要污染源COD、无机氮和活性磷酸盐的分担率场,及各污染源和控制单元的环境容量.研究结果将为该海域入海污染物总量控制提供科学依据.     

卧式螺旋污泥好氧动态堆肥技术的研究

利用卧式螺旋式污泥好氧堆肥装置进行间歇式动态堆肥,对污水厂厌氧消化污泥进行了中温堆肥试验研究.通过控制各组堆肥的含水率、物料配比和通气量,重点探讨各种条件下堆体温度与有机物降解的关系.试验结果表明,厌氧消化污泥以木屑为调理剂在装置中可以实现好氧堆肥处理,其适宜的物料控制参数为:污泥:木屑=10:1～1.5(湿重比),堆肥含水率50%～60%;过程控制参数为:通风量为6.7～8.3 m3/h·t,发酵周期为8 d,温度45℃.     

微波辅助空气氧化水溶液中的PCP

采用活性炭为催化剂,对微波辅助空气氧化水溶液中的五氯酚进行了处理研究.考察了活性炭投加量、微波功率、辐射时间和通气量对溶液中五氯酚的去除率的影响.结果表明,在通气量为0.2 L/min,微波功率800 W和微波辐射60 min时,五氯酚的去除率可达到90%以上;对微波辐射前后的滤液进行紫外扫描和pH分析,可证实五氯酚被降解.     

空气自动监测站的防雷措施

介绍了雷电对空气自动监测站是如何造成危害的，阐述了雷电侵入空气自动监测站的途径及防止雷击的办法。     

A/O脱氮工艺的控制策略和应用性研究

根据A/O脱氮工艺的运行状况和影响因素 ,提出了应用在线传感器连续测定曝气池中DO浓度、氨氮浓度和硝酸氮浓度 ,并据此调节供氧强度、内循环回流量、有机碳源的投加以及硝化区和反硝化区的大小 ,这是保证A/O脱氮工艺良好处理效果的重要控制策略和思想。同时对近年来国外A/O脱氮工艺自动控制的应用及研究进行了简单的回顾。     

Formation of dioxins from combustion of polyvinylidene chloride in a well-controlled incinerator

Polyvinylidene chloride (PVDC; polymer of 1,1-dichloroethylene) was combusted with paper in a well-controlled, small-scale incinerator at an average grate temperature of 700 °C, and then dioxins (PCDDs, PCDFs, and coplanar-PCBs) formed in the exhaust gases were analyzed by gas chromatography/mass spectrometry. PVDC lowered the combustion temperature due to its less flammable character. The amount of total dioxins (PCDDs + PCDFs + coplanar-PCBs) formed in the exhaust gas was 58.0 ng/g of a combustion sample and its toxicity equivalency quantity (TEQ) value was 0.64 ng-TEQ/g. The amount of PCDDs formed in the sample ranged from 2.33 ng/g (Cl₈-isomer) to 0.048 ng/g (Cl₁-isomer). The lower the number of chloride, the less production of PCDDs. On the other hand, there was no relation between the number of chloride and PCDF formation. The amount of PCDFs formed in the sample ranged from 8.02 ng/g (Cl₂-isomer) to 4.46 ng/g (Cl₈-isomer). A polyvinylchloride (PVC) sample produced 207 ng/g of total dioxins and a PVDC sample produced 57.4 ng/g of total dioxins when they were combusted under the same conditions. An approximately equal composition of dioxin isomers was formed from PVDC and PVC samples. Paper was found to contribute to PCDF formation when it was combusted with plastics.     

Vapour pressures, aqueous solubility, Henry's law constants and air/water partition coefficients of 1,8-dichlorooctane and 1,8-dibromooctane

New data on the vapour pressures and aqueous solubility of 1,8-dichlorooctane and 1,8-dibromooctane are reported as a function of temperature between 20 °C and 80 °C and 1 °C and 40 °C, respectively. For the vapour pressures, a static method was used during the measurements which have an estimated uncertainty between 3% and 5%. The aqueous solubilities were determined using a dynamic saturation column method and the values are accurate to within ±10%. 1,8-Dichlorooctane is more volatile than 1,8-dibromooctane in the temperature range covered (p_sat varies from 3 to 250 Pa and from 0.53 to 62 Pa, respectively) and is also approximately three times more soluble in water (mole fraction solubilities at 25 °C of 5.95 × 10⁻⁷ and 1.92 × 10⁻⁷, respectively). A combination of the two sets of data allowed the calculation of the Henry’s law constants and the air water partition coefficients. A simple group contribution concept was used to rationalize the data obtained.     

Occurrences of pharmaceutical and personal care products as micropollutants in rivers from Romania

The occurrence of pharmaceutical and personal care products (PPCPs) was investigated in the Somes River. The aim of this study was to obtain a first overview about the contamination of Somes River (Transylvania) with PPCPs. The samples were preconcentrated by Solid Phase Extraction (SPE) procedures and analysed by GC/MS. A number of 15 compounds including pharmaceutics, metabolites, intermediates and musk fragrances were detected in concentration ranging from 30 ng/l to 10 μg/l. The detected pharmaceuticals are included in following therapeutic groups: analgesics, antiepileptics, psychiatric, stimulants, anticoagulants, antineoplastic and disinfectants.     

Broad range analysis of endocrine disruptors and pharmaceuticals using gas chromatography and liquid chromatography tandem mass spectrometry

Endocrine disrupting compounds (EDCs) and pharmaceuticals and personal care products (PPCPs) have been globally detected in impacted natural waters. The detection of trace quantities of EDCs and PPCPs in the environment is of great concern since some of these compounds have known physiological responses at low concentrations. EDCs can have a wide range of polarities, acidic and basic moieties, and exist in trace quantities, which often requires numerous complex extractions, large sample collection volumes, and multiple instrumental analyses. A comprehensive method has been developed allowing for the analysis of 58 potential EDCs in various water matrices using a single solid-phase extraction (SPE) of a 1 L sample with subsequent analyses using both gas chromatography and liquid chromatography, each coupled with tandem mass spectrometry (GC–MS/MS and LC–MS/MS). Instrument detection limits ranged between 0.12–7.5 pg with corresponding method reporting limits of 1–10 ng l⁻¹ in water. Recoveries for most compounds were between 50% and 112% with good reproducibility (RSD 6–22%).