安全与企业核心竞争力

企业核心竞争力是支撑企业生存发展的根本动力.核心竞争力的不断提升,是企业长久生存和发展的关键.我国安全事故频发,加入WTO和经济全球化迫使我国必须重视职业安全健康非关税壁垒.从企业核心竞争力、安全与核心竞争力的关系以及造成安全生产现状等方面展开论述,并根据核心竞争力的特征以及市场发展现状得出结论,安全必须加入企业核心竞争力的培育中.     

环保法规变化对电力工业发展的影响

从电力需求、发电能源结构、发电能源布局、电力成本及发电技术等方面阐述了环保法规的变化和环境标准的制定对电力工业发展的影响,指出了研究环境保护法规和环境标准趋势的重要性和必要性.     

抗生素废水的铁屑微电解预处理研究

研究了采用铁屑微电解法预处理抗生素废水.在进水COD质量浓度为6.2 g/L时,试验结果表明,经微电解处理后的废水,COD和色度的去除率分别达到68.3%和79.3%,BOD5/COD从0.306提高到0.56,废水的可生化性得到显著提高.通过正交试验考察pH、反应时间及铁屑用量对处理效果的影响,并对各因素作了单因素影响试验,确定了最佳工艺条件.     

新民市柳河水源地水环境健康风险评价

为了评价新民柳河水源地的供水安全,简要介绍水环境健康风险评价基本方法的基础上,建立了水环境健康风险评价模式.研究结果表明:①柳河水源地地面水基因毒物质为优先控制污染物;而地下水应着力控制躯体毒物质.②对于基因毒物质,监测断面优先控制污染物为As和Cr;而对于躯体毒物质,所有监测断面的优先控制污染物均为氨.③在所有监测断面中,柳河上断面等6处有毒污染物所致健康危害的个人年总风险数量级为10-5-10-4.在日后的管理过程中,应对这6处加大治理力度.④目前环境健康风险评价还没有包括在常规环境评价工作中,建议在今后的评价工作中应该逐步开展这方面的工作,以提高供水安全.     

有机酸性腐蚀品生产危险性分析

目前我国化工生产中涉及大量有机酸性腐蚀品,通过对某市化工行业调查及分析,发现有机酸性腐蚀品生产普遍,而且生产原料易燃易爆,生产过程存在火灾爆炸危险,结合具体生产工艺,采用预先危险性分析法和作业条件的危险性评价法分析生产过程危险性,从而揭示并概括有机酸性腐蚀品生产危险性.为更好地促进我国安全生产,在此基础上探讨了一些针对性的安全措施.     

基于无人机多传感吊舱系统的火点实时定位方法

林火定位是林火智能监测设备的核心技术。提出了一种基于激光雷达、红外热像仪及组合惯导多数据融合的火点定位方法。首先设计了一个通用的无人机吊舱系统,并基于ROS框架实现数据采集、数据处理和数据传输等功能;其次提出了一个基于无人机吊舱系统的火点全局定位方案,根据红外热像仪成像特性识别火点,同时将密集点云与红外图像进行数据融合,估计出火点的三维空间位置;然后根据无人机位姿提出了一种基于墨卡托投影的火点全局定位方案,得到了火点的GPS位置。最后通过试验得到了该方案的全局定位精度：在实验中经度最大误差为2.36×10^-5°,纬度最大误差为1.84×10^-5°,高程最大误差为0.926 1 m,为其他林火定位方案提供了技术支持。     

Causes of change in nitrophytic and oligotrophic lichen species in a Mediterranean climate: impact of land cover and atmospheric pollutants

With the aim of determining the main drivers of changes in nitrophytic and oligotrophic macro-lichen communities in an industrial region with a Mediterranean climate, we considered both land-cover types and atmospheric pollutants. We determined the relation between the abundance of nitrophytic and oligotrophic species with environmental factors considering the distance of influence of land-cover types. The results showed that oligotrophic species decreased in the proximity of artificial areas, barren land and agricultural areas, associated with higher concentrations of NO₂ and Zn, and Ti, probably dust of industrial and agricultural origin. Nitrophytic species were positively related to all the mentioned land-cover types, and with higher concentrations of Fe and N. Magnesium, probably from ocean aerosols, was negatively related to oligotrophic species and positively to nitrophytic.     

A2/O工艺中的反硝化除磷

A2/O工艺是一种最简单的同步脱氮除磷工艺,但由于其系统中固有的基质竞争和污泥龄等矛盾,在实际应用中特别是处理低C/N比污水时脱氮除磷效率较低.反硝化除磷工艺作为近年来颇受关注的污水生物处理新技术.由于在脱氮除磷过程中可以在碳源利用上耦合,可从一定程度上缓解A2/O工艺中的基质竞争矛盾,使得其在处理低C/N比污水时也能实现较高的脱氮除磷效率.就反硝化除磷的技术原理,结合其在A2/O工艺中的最新研究成果及其控制策略,对A2/O工艺中的反硝化除磷的实现、维持及影响因素进行了分析和探讨,并对其发展方向进行了展望.     

Monitoring air quality with lichens: a comparison between mapping in forest sites and in open areas

Four different methods of epiphytic lichen mapping were used for the assessment of air quality in the region under the influence of the Sostanj Thermal Power Plant (Salek Valley, Slovenia). Three methods were based on the presence of different lichen species (VDI, EU and ICP-Forest), the fourth on a frequency and coverage assessment of different growth forms of epiphytic lichens, e.g. crustose, foliose and fruticose (SI). A comparison of the results from the assessment of air quality between forest sites (ICP-Forest, SI) and open areas (VDI, EU and SI), obtained by the different methods of epiphytic lichen mapping, is presented in the contribution. Data showed that lichen species richness is worse in forest sites in comparison with open areas. From the data obtained it can be concluded that epiphytic lichen mapping in open areas is a better method for the assessment of air pollution in a given area than mapping in forest sites. The species-based methods in open areas are more powerful and useful for air quality assessment in polluted research areas than the SI and ICP-Forest methods.     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.