盐效萃取法从电子产品清洗废液中回收异丙醇

用盐效萃取法从电子产品清洗废液中回收片丙醇,考察了碳酸钾水溶液与该清洗废液的质量比对脱水率的影响,测定了异丙醇-水-碳酸钾体系存40℃时的液液相平衡数据,用Pitzer理论和NRTL方程对液液相平衡数据进行了理论计算。结果表明：当质量分数为60．00％的碳酸钾水溶液与该废液的质晕比为2．00时,脱水率高达90．00％;将有机相进行精馏可得到质量分数为99．50％的异丙醇;计算值与实测值接近,水相和有机相的绝对平均偏差分别为0．62％和0．46％。     

Identifying the largest individual sample value from a two-way composite sampling design

Composite sampling techniques for identifying the largest individual sample value seem to be cost effective when the composite samples are internally homogeneous. However, since it is not always possible to form homogeneous composite samples, these methods can lead to higher costs than expected. In this paper we propose a two-way composite sampling design as a way to improve on the cost effectiveness of the methods available to identify the largest individual sample value.     

一种基于预测法的电磁兼容设计方法

文章以数模混合电路设计实践为基础,介绍了一种基于预测法的电磁兼容设计方法。先以电磁兼容测试理论为基础介绍数模混合电路设计中的电磁兼容方法,在以此方法建立电磁兼容设计模型,并通数模混合电路实践来检验和改进设计模型。     

大港油田苦咸再生水反渗透工艺自动控制研究

分析了大港油田污水回用深度处理工程苦咸再生水反渗透工艺仪表配置及自动控制方式,介绍了苦咸再生水反渗透系统亟待解决的各类问题。着重论述了仪表设置、余氯控制、结垢污堵控制、微生物污堵控制的实际运行方式,探讨了苦咸再生水反渗透工艺的技术可行性和可靠性。     

Subcritical water oxidation of propham by H2O2 using response surface methodology (RSM)

This study was conducted to investigate the degradation of propham, which is a compound that pollutes water and seriously threatens human health, by subcritical water oxidation and using H₂O₂ as an oxidising agent. The maximum total organic carbon removal rate of propham was obtained as 73.65% at 40 min of treatment time and 60 mM of H₂O₂ concentration and 373 K of temperature. In addition, response surface method based on the Box-Behnken design was applied to design the degradation experiments of propham for determination of the combined effects of process variables, namely temperature, concentration of oxidising agent and treatment time. The proposed quadratic model of propham degradation, which was examined with the analysis of variance, was used for navigating the design space. The R² and adjusted R² values of the model were determined as 0.9921 and 0.9819 respectively. It was shown that propham was effectively degraded, thus could be removed from the water by using an environmentally friendly method.     

天然气引射调峰系统的噪声形成及其治理研究

采用天然气引射调峰技术,能使上海某储配站10台天然气高压球罐的储气调峰能率提高68%,大大有助于解决天然气用气高峰时的供需平衡问题,并能节约初投资人民币1亿元.但使用超音速引射器后,当球罐压力下降到某一值时会产生高频噪声,影响管束区操作环境.本文分析了噪声产生的原因,提出了合理的噪声治理方案,并进行了方案的实施.实践证明:噪声治理效果良好,降低了管束区噪声污染,达到了国家"工业企业噪声卫生标准".     

SBR法处理豆制品废水工艺条件的研究

用SBR法处理豆制品废水的试验表明,该系统具有较好的抗负荷冲击能力,进水COD在300～2000 mg/L之间变化,对系统不造成任何影响;考察了曝气时间、曝气量和污泥浓度等对去除效果的影响,试验结果表明,曝气时间和曝气量对处理效果影响很大,确定该反应系统最佳曝气时间是8 h,适宜的曝气量是800 L/h,而污泥浓度控制在4000 mg/L左右时,处理效率最高,采用进水顶出水的排水方式是可行的,确定系统的最佳排水比是3/5.厌氧段的插入可以减少剩余污泥的产量.     

试论环境侵害损害赔偿中的行政调解

论述了环境侵害损害赔偿中应用行政调解的特点、效力等问题，具有一定的现实意义。     

Contribution of anthropogenic pollutants to the increase of tropospheric ozone levels in the Oporto Metropolitan Area, Portugal since the 19th century

The main purpose of this study was to evaluate the contribution of anthropogenic pollutants to the increase of tropospheric ozone levels in the Oporto Metropolitan Area (Portugal) since the 19th century. The study was based on pre-industrial and recent data series, the results being analyzed according to the atmospheric chemistry. The treatment of ozone and meteorological data was performed by classical statistics and by time-series analysis. It was concluded that in the 19th century the ozone present in the troposphere was not of photochemical origin, being possible to consider the respective concentrations as reference values. For recent data a cycle of 8h for ozone concentrations could be related to traffic. Compared to the 19th century, the current concentrations were 147% higher (252% higher in May) due to the increased photochemical production associated with the increased anthropogenic emissions.     

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%).