入世十年我国对外贸易的宏观环境影响研究

入世十年来,我国对外贸易迅猛发展,贸易价值量取得巨大顺差,但其背后却孕育着巨大的资源环境逆差。本文通过建立贸易的环境核算方法,运用我国"能源-经济-环境"投入-产出及CGE模型分析了2002、2005、2007年的投入产出表,对进出口产品虚拟污染物进行定量核算,衡量入世十年我国对外贸易的宏观环境影响。研究表明,入世十年来,我国净出口产品虚拟SO2排放约占全国排放总量的1/4;净出口产品虚拟CO2排放占全国排放总量超过30%;净出口产品COD排放占全国排放总量的20%以上。在不采取其他措施的情况下,我国在未来20年仍将处于巨大的贸易环境逆差之中。     

农药对藻类的生态毒理学研究Ⅰ:毒性效应

随着现代农业的发展,世界范围内使用的农药品种越来越多,用量不断增加。农药对非靶生物的影响以及农药残留导致环境污染,造成生态系统结构和功能的破坏,早已受到了国内外的广泛关注。有关农药对生态系统中消费者类群毒性效应的研究较多。近年来,农药对于生态系统初级生产者－ 藻类的毒性及其生态毒理学的研究倍受重视。大力开展这方面的研究对于深入了解农药在生态系统中的迁移、转化及整体生态效应以及农药的生态风险评价无疑具有重要的理论意义和应用价值。本文综述了近年来国内外有关农药对单种藻类和藻类群落的毒性效应,影响毒性的环境因子。     

性能化火灾安全评估应用个案研究

性能化火灾安全评估屉当前火灾科学及其应用研究的热点之一。该方法利用火灾动力学、热化学、安全评估原理学等确定性工程方法，针对各类建筑的结构特点和实际状况，对建筑物的火灾危险进行定性的预测和评估。以某高层建筑的维修工程为例，评估了其维修期间的火灾安全水平。通过对其维修前（满足规范要求）和维修期间（不满足规范要求）两种情况下人员疏散过程的比较，并辅以烟气运动规律的预测，得出了该建筑在施工期间的安全水平。     

环境治理中光催化剂的失活与再生

催化剂失活是影响光催化过程用于污染治理经济实用的关键因素。对近几年来国内外环境污染控制中光催化剂的失活现象及其原因进行了综述．分析了液相和气相光催化反应体系中催化剂失活后再生的方法．特别是对气相光催化反应中水蒸汽的影响进行了讨论。     

电子垃圾拆解回收VOCs排放特征与排放因子

电子垃圾拆解回收过程中的高温处理往往产生大量挥发性有机物(VOCs),对周边环境及人体健康产生不可忽视的影响.本研究选取某电子垃圾集中拆解回收场,对场区加热烤板车间、塑料制粒车间、湿法提取车间和火法冶炼车间废气处理设施排放口的VOCs浓度和组分进行监测,分析了不同生产工艺VOCs排放特征及其总VOCs排放因子.结果表明...     

越江电力地下综合管廊结构横向抗震性能研究∗

针对越江气体绝缘输电线路(GIL)综合管廊结构的特殊性,考虑内部混凝土支架与盾构隧道的动力相互作用,以及盾构隧道穿越地层的不同,建立了土?管廊结构非线性动力相互作用的整体计算分析模型,从结构变形、盾构管片张开量、结构地震损伤等方面详细分析了越江 GIL 综合管廊结构的抗震性能。结果表明：越江 GIL 管廊结构内部混凝土支架结构明显要先于外部盾构隧道发生地震损伤;当 GIL 管廊结构穿越相对较软土层时的地震损伤明显加重;受制于内部混凝土支架的约束作用,盾构隧道的下部管片张开量明显小于上部管片计算值,同时外侧残余张开量要明显大于管片内侧残余张开量。     

昌江核电站运营前附近海域总β放射性水平

在昌江核电站运营前,研究人员对其附近海域做了水质、沉积物和海洋生物总β放射性调查,并与我国其他海域及昌江核电站周围的陆地环境做了对比。结果表明:（1）海水样品总β比活度范围为0.040～0.074 Bq/L,平均值为0.054 Bq/L,与渤海、黄海、东海、南海近海、大亚湾核电站等海域相比,昌江核电站海域海水中总β放射性水平相对较低;（2）表层沉积物中总β比活度范围为257～925 Bq/kg,平均值为653 Bq/kg,研究海域沉积物中总β放射性水平与香港、青岛、阳江等海域水平相当;（3）海洋生物样品中总β比活度范围为8.7～63.8 Bq/kg,平均值为48.0 Bq/kg,海鱼类、虾类和贝类体内总β平均值分别为56.7 Bq/kg、63.4 Bq/kg和24.0 Bq/kg,鱼类和虾类明显大于贝类。本研究可为今后科学、合理地评价核电站运行对海洋环境的影响提供重要的数据支撑。     

Effects of Zr substitution on soot combustion over cubic fluorite-structured nanoceria: Soot-ceria contact and interfacial oxygen evolution

Ceria is widely used as a catalyst for soot combustion, but effects of Zr substitution on the reaction mechanism is ambiguous. The present work elucidates effects of Zr substitution on soot combustion over cubic fluorite-structured nanoceria. The nanostructured CeO₂, Ce_0.92Zr_0.08O₂, and Ce_0.84Zr_0.16O₂ composed of 5–6 nm crystallites display T_m-CO2 (the temperature at maximum CO₂ yield) at 383, 355, and 375°C under 10 vol.% O₂/N₂, respectively. The size of agglomerate decreases from 165.5 to 51.9–57.3 nm, which is beneficial for the soot-ceria contact. Moreover, Zr increases the amount of surface oxygen vacancies, generating more active oxygen (O₂^? and O^?) for soot oxidation. Thus, the activities of Ce_0.92Zr_0.08O₂ and Ce_0.84Zr_0.16O₂ in soot combustion are better than that of CeO₂. Although oxygen vacancies promote the migration of lattice O^2?, the enriched surface Zr also inhibits the mobility of lattice O^2?. Therefore, the T_m-CO2 of Ce_0.84Zr_0.16O₂ is higher than that of Ce_0.92Zr_0.08O₂. Based on reaction kinetic study, soot in direct contact with ceria preferentially decomposes with low activation energy, while the oxidation of isolated soot occurs through diffusion with high activation energy. The obtained findings provide new understanding on the soot combustion over nanoceria.     

Kinetics of aniline oxidation with chlorine dioxide

For the first time, kinetics of aniline oxidation with chlorine dioxide(ClO2) were investigated systematically by detecting concentration of aniline with HPLC at regular intervals. Results showed that the reaction was first-order both in ClO2 and in aniline, and the oxidation reaction could be described as second-order reaction. Stoichiometric factor η was experimentally determined to be 2.44. The second-order-reaction rate constant k was 0.11L/(mol.s)under condition of pH 6.86 and water temperature(Tw) 287K. Reaction activation energy was 72.31 kJ/mol, indicating that the reaction could take place under usual water treatment conditions. The reaction rate constants in acidic and alkali media were greater than that in neutral medium. Chlorite ion could slightly increase reaction rate in acidic medium. p-aminophenol and azobenzene were detected by GC-MS as intermediates.     

Flammability of heat transfer fluid aerosols produced by electrospray measured by laser diffraction analysis

Accidental release of pressurized high flash point heat transfer fluids can result in fire and explosion hazard scenarios in the process industry. An experimental investigation on ignition of aerosols of a heat transfer fluid is carried out, and characterization of aerosol and its ignition process by non-intrusive laser diffraction technique is reported. Propagation speed of the aerosol combustion flame front as analyzed from the laser diffraction measurement agrees with high-speed visual camera observation. Flammability of the aerosol, which is based on the chances of the global flame appearance in the aerosol, is mainly controlled by aerosol droplet size and the droplet volume concentration.