危机管理体制构建与政府职能转变--后非典时期对于突发公共灾害处置的思考

本文以公共卫生危机和社会突发事件为个案,以政府面对这些危机所面临的挑战和取得的经验为研究对象,分析公共危机产生的原因和基本特征,提出了面对公共危机时应建立政府危机管理的预警系统,建立快速反应机制,动员社会参与危机救治,加强信息流通,加强公共危机的法制化建设.     

嗜热微生物在废水处理中的应用

利用嗜热微生物处理高温排放废水是一项很有前任的废水处理技术，文章对嗜热微生物好氧处理废水及厌氧处理废水的发展进程和研究现状做了综述，例举了嗜热微生物在废水处理中的应用，并论证了一定工艺条件下高温废水处理的可行性和优越性；最后对嗜热微生物在废水处理中的应用前景作了展望。     

华北平原分区适宜性农业节水技术与潜力

华北平原现状农田灌溉水利用率为43 1 % ,节水潜力较大。论文通过分区诊断与适应性农业节水技术评价计算 ,提出了2010年和2030年水平年分区适宜性农业节水技术发展的综合排序 ,并以现状为基点 ,计算与分析了两个水平年分区不同农田灌溉技术的发展规模和相应的节水量     

Rh-Al-MCM-41上NO选择性催化还原的原位红外研究

利用气-固相固定床反应装置考察了Rh交换的Al-MCM-41在高气体空速条件下对贫燃NOx的选择性催化还原活性,考察了氧含量对其的影响。结果表明,在200000h~(-1)的气体空速、O_2/C_3H_6=20、603K时,NO转化率为74.3％。利用原位FTIR技术研究了该催化剂的表面吸附物种及表面程序升温反应行为,并结合实验观察探讨了贫燃条件下Rh-Al-MCM-41催化剂上NO的选择性催化还原机理。     

炼化装置大型机组润滑油站油雾回收系统改造

针对炼化装置机组润滑油站油雾无法回收、现场卫生差及VOCs排放超标等问题,通过对几种油雾治理方式的分析比对发现,将离心式分离法和过滤法相结合可显著降低补油量,改善现场卫生,直接减少非甲烷总烃排放量,同时也为装置创造了一定的经济效益。     

碳氮结构空心管材料及其对钍离子的吸附性能研究

目的合成碳氮结构空心管材料,用于稀土矿山开采中放射性钍离子的吸附去除,方法通过三聚氰胺和三聚氰酸超分子自组装,经水热碳化及高温热解,制备碳氮结构空心管材料.采用SEM、XRD等对材料进行表征.在不同热解温度和pH值下进行钍离子吸附实验,比较不同钍离子的初始浓度和吸附时间下吸附容量的差异.结果600℃时,材料形貌为均匀的中空管状结构;pH=3.5,热解温度为800℃时,材料最大吸附容量达到133.87 mg/g,吸附过程符合Langmuir等温吸附模型且遵从准二级动力学规律.结论碳氮结构空心管材料对钍离子具有良好的吸附效果,有望用于稀土开采过程中产生的放射性废钍离子的去除.     

Indirect effect of nutrient accumulation intensified toxicity risk of metals in sediments from urban river network

The levels of metals in sediments of urban river ecosystems are crucial for aquatic environmental health and pollution assessment. Yet little is known about the interaction of nutrients with metals for environmental risks under contamination accumulation. Here, we combined hierarchical cluster, correlation, and principal component analysis with structural equation model (SEM) to investigate the pollution level, source, toxicity risk, and interaction associated with metals and nutrients in the sediments of a river network in a city area of East China. The results showed that the pollution associated with metals in sediments was rated as moderate degree of contamination load and medium-high toxicity risk in the middle and downstream of urban rivers based on contamination factor, pollution load index, and environmental toxicity quotient. The concentration of mercury (Hg) and zinc (Zn) showed a significant correlation with toxic risks, which had more contribution to toxicity than other metals in the study area. Organic nitrogen and organic pollution index showed heavily polluted sediments in south of the study area. Though correlation analysis indicated that nutrients and metals had different input zones from anthropogenic sources in the urban river network, SEM suggested that nutrient accumulation indirectly intensified toxicity risk of metals by 13.6% in sediments. Therefore, we suggested the combined consideration of metal toxicity risk with nutrient accumulation, which may provide a comprehensive understanding to identify sediment pollution.

Toxicity rate of metals in sediments from urban river network indirectly intensified by nutrients accumulation

     

Effect of organic acids on adsorption and desorption of rare earth elements

Effect of citric, malic, tartaric and acetic acids on adsorption of La, Ce, Pr and Nd by and desorption from four typical Chinese soils was studied. Generally, adsorption capacities of rare earth elements (REEs) were significantly correlated with the cation exchange capacity (CEC) of soils. In the presence of acetic acids adsorption of REEs was similar to that in the presence of Ca(NO3)2. However, in the presence of citric, malic and tartaric acids adsorption of REEs by Heilongjiang, Zhejiang and Guangdong soils decreased to varying extents if compared with that in the presence of nitrate and acetic acid. The significance of suppression followed the order of citric acid > malic acid > tartaric acid > acetic acid, which was consistent with the order of stability of complexes of REEs with these organic acids. However, the adsorption increased with increasing equilibrium solution pH. For Jiangxi soil with low soil pH, CEC and organic matter these organic acids exerted an even more serious suppression effect on the adsorption of REEs. Another feature of the relationship between the adsorption of REEs and equilibrium solution pH was that the adsorption of REEs decreased with increase of pH from 2 to 4.5 and then slightly increased with further increase of pH. Desorption of REEs varied with soils and with organic acids as well. REEs were released easily from Heilongjiang, Zhejiang and Guangdong soils in the presence of organic acid. Generally, desorption of REEs decreased with increasing equilibrium solution pH. Effect of organic acids on desorption of REEs from Jiangxi soil was more complicated. In the presence of citric and malic acids no decrement and/or slight increase in desorption of REEs were observed over the equilibrium solution pH from 3 to 6.5. The reasons for this were ascribed to the strong complexing capacity of citric and malic acids and low soil pH, CEC and organic matter of Jiangxi soil.     

Comparison of a rhizosphere-based method with other one-step extraction methods for assessing the bioavailability of soil metals to wheat

There is no method recognized as a universal approach for evaluation of bioavailability of heavy metals in soil. Based on the simulation of the rhizosphere soil conditions and integration of the combined effects of root-soil interactions as a whole, a rhizosphere-based method has been proposed. Wet fresh rhizosphere soil was extracted by low-molecular-weight organic acids (LMWOAs) to fractionate metal fractions of soil pools, which were then correlated with the metal contents of wheat roots and shoots. The rhizosphere-based method was compared with other one-step extraction methods using DTPA, EDTA, CaCl2, and NaNO3 as extractants and the first step of the Community Bureau of Reference (BCR) method. Simple correlation and stepwise multiple regression analysis were used for the comparison. Simple correlation indicated that the extractable Cu, Zn, Cr, and Cd of soils by the rhizosphere-based method were significantly correlated with the metal contents of wheat roots. For DTPA, BCR1 and EDTA methods there was a relatively poor correlation between the extractable Cu, Zn and Cd of soil and metal contents of wheat roots. Stepwise multiple regression analysis revealed that the equation of the rhizosphere-based method was the simplest one, and no soil properties variables needed to be added. In contrast, the equations of other one-step extraction methods were more complicated, and soil properties variables needed to be entered. The most distinct feature of the rhizosphere-based method was that the recommended method was suitable for acidic, neutral and near alkaline soils. However, the DTPA and EDTA extraction methods were suitable for calcareous soils only-or-only for acidic soils. The CaCl2, and NaNO3 extraction methods were only suitable for exchangeable metals. In short, the rhizosphere-based method was the most robust approach for evaluation of bioavailability of heavy metals in soils to wheat.     

A model for evaluation of the phytoavailability of trace elements to vegetables under the field conditions

Currently, several single extraction methods are used for the evaluation of the phytoavailability of metals using pot experiments. A systematic comparison, however, is lacking. It is especially true for the field studies. This study was to investigate the phytoavailability of trace elements to vegetables grown on metal-contaminated soils under the field conditions. All soils collected were typical calcareous soils in northern China. Four frequently used methods using CaCl2, diethylenetriaminepentaacetic acid (DTPA), CH3COOH, and water as extractants were compared for phyto-availability. The concentrations of metals extracted by these four extraction methods ranged from 3.42 to 815, 1.51- 6965, 0.732-24473, 0.688-7863, 0.246-685, 1.99-5337 0.203-4649 ng/g for Cr, Ni, Zn, Cu, Cd, Pb and REEs, respectively. Simple correlation analysis indicated that a significant correlation (Cr: r = 0.5411**; Zn: r = 0.6352**; Cd: r = 0.6979**; Pb: r = 0.5537** and REEs: r = 0.5185** -0.6684**) was observed between the CaCl2-extractable metals in soil solution and that in Chinese cabbage. In addition, soil pH, organic matter (OM), and cation exchange capacity (CEC) also affect the phytoavailability. An empirical model was developed to express the combined effect of soil properties on the phytoavailability. The stepwise multiple regression analysis demonstrated that the phytoavailability of trace elements strongly correlated with the extractable fraction by CaCl2, total metal concentration in soils, and soil pH, OM, CEC. This model can describe approximately 75-95% of the variability of metal uptake and the r2 values ranged from 0.741** to 0.954**, which were much better than the single correlation analysis. For celery and cole, a strong correlation was obtained for Cr, Ni, Zn, Cu, Cd, La, Ce, Pr and Nd. For spinach and Chinese cabbage, however, a positive correlation was only observed for 1 and 3 metals, respectively. Generally, the developed empirical model can integrate the combined effects of soil properties, extractable metal fractions in soil solutions and plant species on the phytoavailability of metals to vegetables in the field conditions.