城市危险化学品事故统计分析与对策

通过对2002-2004年发生在中国内地12个主要城市的435起非爆炸品类危险化学品事故统计分析,发现:(1)危险化学品事故总体呈进一步发展趋势;(2)处于城市生活区的化工企业发生危险化学品事故对城市的影响最大;(3)危险化学品在运输阶段,发生事故的比例最高;(4)民用燃气是造成使用阶段危险化学品事故的主要危险源,而人为失误和违规操作是民用燃气类危险化学品事故的主要原因.在统计分析基础上提出了相应的对策.     

Combination with catalyzed Fe(0)-carbon microelectrolysis and activated carbon adsorption for advanced reclaimed water treatment: simultaneous nitrate and biorefractory organics removal

A process combining catalyzed Fe(0)-carbon microelectrolysis (IC-ME) with activated carbon (AC) adsorption was developed for advanced reclaimed water treatment. Simultaneous nitrate reduction and chemical oxygen demand (COD) removal were achieved, and the effects of composite catalyst (CC) addition, AC addition, and initial pH were investigated. The reaction kinetics and reaction mechanisms were calculated and analyzed. The results showed that CC addition could enhance the reduction rate of nitrate and effectively inhibit the production of ammonia. Moreover, AC addition increased the adsorption capacity of biorefractory organic compounds (BROs) and enhanced the degradation of BRO. The reduction of NO₃^?–N at different pH values was consistently greater than 96.9%, and NH₄⁺–N was suppressed by high pH. The presence of CC ensured the reaction rate of IC-ME at high pH. The reaction kinetics orders and constants were calculated. Catalyzed iron scrap (IS)-AC showed much better nitrate reduction and BRO degradation performances than IS-AC and AC. The IC-ME showed great potential for application to nitrate and BRO reduction in reclaimed water.

     

Remobilization of polycyclic aromatic hydrocarbons during the resuspension of Yangtze River sediments using a particle entrainment simulator

Remobilization of 16 polycyclic aromatic hydrocarbons (PAHs) during sediment resuspension was investigated using a particle entrainment simulator at shear stress from 0.2 to 0.5Nm(-2), typical of the energy levels present in many tidally driven aquatic environments. The results suggested that desorption from the entrained particles was the primary source of dissolved PAHs. summation operatorPAHs concentrations in particles on volume normalization increased about four times. However, on mass weight basis, summation operatorPAHs concentrations decreased from 6039.74+/-138.28microgkg(-1) to 1665.39+/-112.26microgkg(-1). The same trend was observed for individual PAHs. Dissolved concentrations of PAHs demonstrated significant differences depending on molecular weight and applied shear. The distribution of PAHs between particle and water phase suggested that for three-ring PAHs, the amounts of PAHs in particles were higher than the predicted values during our experiments. This might be due to presence of another active sorbent.     

Investigation into organic phosphorus species in sediments of Baiyangdian Lake in China measured by fractionation and 31P NMR

Organic phosphorus (OP) species in sediments of the Baiyangdian Lake in China was investigated via fractionation and phosphorus-31 nuclear magnetic resonance ((31)P NMR) spectroscopy. Results of chemical fractionation showed that different OP fractions ranked in the order: humic acid-P?>?HCl-OP?>?fulvic acid-P?≈?NaHCO(3)-OP?>?residual OP. Labile OP and moderately labile OP, which can be degraded for phytoplankton uptake, contributed to 58.7-68.5% of total extracted OP, indicative of the potential P release from sediments in the lake. (31)P NMR spectroscopy results suggested the rank order of P species present in the NaOH-EDTA extractant of the sediments: orthophosphate?>?monoester-P?>?DNA-P?>?pyrophosphate-P. Phytate, polyphosphates, and phosphonates, which appeared in sediments of some deeper lakes, were not detected in the shallow lake. Significant correlations were identified between total P (TP) in water column and sediment TP, monoester-P and DNA-P, positively indicating that sediment P species, especially OP components, should probably contribute to the contents of P in water column and further to the lake eutrophication.     

Preliminary Strategic Environmental Assessment of the Great Western Development Strategy: Safeguarding Ecological Security for a New Western China

The Great Western Development Strategy (GWDS) is a long term national campaign aimed at boosting development of the western area of China and narrowing the economic gap between the western and the eastern parts of China. The Strategic Environmental Assessment (SEA) procedure was employed to assess the environmental challenges brought about by the western development plans. These plans include five key developmental domains (KDDs): water resource exploitation and use, land utilization, energy generation, tourism development, and ecological restoration and conservation. A combination of methods involving matrix assessment, incorporation of expert judgment and trend analysis was employed to analyze and predict the environmental impacts upon eight selected environmental indicators: water resource availability, soil erosion, soil salinization, forest destruction, land desertification, biological diversity, water quality and air quality. Based on the overall results of the assessment, countermeasures for environmental challenges that emerged were raised as key recommendations to ensure ecological security during the implementation of the GWDS. This paper is intended to introduce a consensus-based process for evaluating the complex, long term pressures on the ecological security of large areas, such as western China, that focuses on the use of combined methods applied at the strategic level.     

林可霉素菌(Streptomyces lincolnensis)利用吡唑酮废水的研究

采用被吡唑酮废液驯化、分离、筛选后的林可霉素菌,并对其在摇瓶上利用吡唑酮废液中的硫酸铵发酵(7 d)生产林可霉素进行了研究。实验结果表明,废液加入培养基体积比都为1∶10,实验1中菌丝代谢和对照比正常,其中还原糖利用最快,在发酵后期为0.24 mg/L,林可霉素起步效价最低为2 100 IU/mL,与对照相比最后发酵效价降低了70 IU/mL;实验2发酵过程pH值偏低,全程为5.86～6.50,氨基氮代谢缓慢为40 mg/100 mL,最后林可霉素效价最低为4 480 IU/mL;实验3中废液在发酵进入48 h中后期的时候补入能促进菌丝体分泌,最后林可霉素为5 180 IU/mL,比对照发酵水平高出8.82%。可见实验3的实验设计有利于林可霉素菌利用吡唑酮废液生产林可霉素,为废物循环利用、变废为宝的可行性作了有意义尝试。     

烧结机头除尘灰生产复合肥的研究

通过系统分析烧结机头除尘灰的成分和化学结构,研究制定了利用烧结除尘灰生产复合肥的配方和工艺,该研究为烧结除尘灰的利用开发了新的用途。     

Temperature-dependent sorption of polycyclic aromatic hydrocarbons on natural and treated sediments

In aqueous environment temperature is considered to play a significant role in the sorption process of polycyclic aromatic hydrocarbons (PAHs) and its influence on the sorption equilibrium is indicative of sorption energies and mechanisms. In this study, sorptions of five PAHs on three heterogeneous sorbents including one river sediment (YHR), one estuary sediment (YRD) and one treated sediment with organic matter removed (IM) were carried out at a range of temperature from 5 °C to 35 °C. Stronger sorptions were observed at lower temperatures, with the equilibrium sorption coefficient K_d increasing 2-5 times as the temperature decreases 30 °C. The increase of K_d value was attributed primarily to the change of PAH water solubility, which predicted 40-75% of the increase of K_d in the sorption process. To provide insight into the sorption mechanism, enthalpy change (ΔH_S) for the sorption process was calculated and the values were observed to be negative for all of the interactions, suggesting that the exothermal sorption of PAHs inversely dependents on temperature. Based on the values of ΔH_S, van der Waals forces were inferred as the main sorption mechanism for the PAHs, especially on the YHR sediment which contained more organic matter. For sorption of larger size PAHs on the sorbents with low organic matter, specific interactions were deduced to contribute to the overall sorption.     

超临界CO2流体环境中线路板分层实验分析

在超临界CO2流体环境下,当温度达到240℃以上时,印刷线路板就会发生分层现象。同时,在实验中发现在非超临界流体环境下,当温度达到260℃以上时,线路板也会发生分层现象。从线路板粘接材料发生热解反应的角度出发,在对比超临界CO2流体环境下与非超临界流体环境下的线路板分层效果的基础上,对超临界CO2流体环境下的线路板分层...