氮、磷吸附/解吸法确定环保疏浚深度方法探讨——以太原汾河示范段为例

有效疏浚深度是决定疏浚工程造价和治理效果的关键指标,目前我国现行标准规范尚未明确底泥营养盐浓度的标准,对营养盐超标河湖污染底泥的评价和有效疏浚深度确定十分不利。以太原汾河示范段为例,取其代表性柱状样0.3~0.4、0.9~1.0、1.4~1.6、1.9~2.0 m深度的底泥,分别设计Ⅰ类~劣Ⅴ类氨氮( N H 4 + -N)、正磷酸盐( P O 4 3 - )的模拟水和柱状样实际上覆水,进行氮、磷吸附/解吸试验,并分析不同深度底泥氮、磷吸附/解吸特征。结果表明:柱状样1.6 m深度以内底泥中 NH 4 + -N对水体呈释放状态,1.9 m深度底泥对水体中 NH 4 + -N具一定吸附性;1.6 m深度以内底泥中 PO 4 3 - 对水体有释放风险,1.9 m深度底泥对水体中 PO 4 3 - 具一定吸附性;1.3 m深度底泥中总氮(TN)、 NH 4 + -N浓度出现较明显的拐点,1.6 m深度底泥中总磷(TP)浓度出现较明显的拐点。结合底泥对上覆水体影响及底泥中氮、磷浓度垂向变化等因素,确定太原汾河示范段有效疏浚深度为1.6 m。     

贸易对环境影响的初步研究

根据环境经济系统的双层结构建立了贸易对环境影响的概念模型 ,即贸易通过环境类、经济类物品和服务的输入输出 ,对环境子系统直接或通过经济子系统间接产生影响 ;对影响环境的贸易 (外部因素 )与环境成本内部化(内部因素 )问题 ,分别进行了分析 ;就贸易对环境影响的研究方法问题 ,运用局域均衡模型 ,为局域贸易环境问题的量化分析提供较为便捷、可靠的模式进行了初步探讨。     

政府环境规制下的企业治理动机与公众参与外部性研究

本文构建了多主体参与环境治理的动态一般均衡模型,进行了政府环境规制下的企业内生治理动机研究与公众参与外部性的分析,模拟结果显示,企业内生治理动机、社会福利等不同目标下对应的最优环境税率存在明显差异。随着政府环境税率的不断上升,企业环境技术研发投入会先上升后下降,当环境研发投入水平达到最大时,政府所征收的环境税完全激发了企业的内生治理动机。在环境税率提高的初期,研发引致的环境技术进步使得企业的全要素生产率得以提高,经济产出不断增加,社会福利水平得到增进。当环境税率上升到一定数值之后,环境税带来的资源配置扭曲效应高于环境负外部性的改善效应,对于经济而言,环境税成为扭曲性税收,并会降低社会福利水平。因此,应在保证经济增长和社会福利增进的同时有效激励企业内在治理动机,将环境税率设定在适当水平。本文还模拟了政府与公众参与的组合对于社会福利的影响情况,与仅考虑政府环境规制政策的情形相对比,政府征收环境税和社会组织参与的共同作用可以使得社会福利提高,充分表明了公众参与环境治理存在着正外部性。环境社会组织在一定程度上可以降低政府信息不对称等因素,改善环境治理状况。环境组织的参与还能够使得环境税所带来的环境治理改善和生产效率提高的双重红利逐渐释放。因此,在发挥政府规制与市场调节功能的同时,充分发挥环境社会组织和公众在环境治理中的作用,是改善环境质量、提高公众福利的重要方式。     

Marked disequilibrium between 234Th and 230Th of the 238U natural radioactive decay chain in IAEA reference materials n. 312, 313 and 314

A new laboratory for the spectroscopy of natural radioactivity with a good energy resolution is presented. It consists of two distinct parts equipped, respectively, the first one with a HpGe γ-ray detector, whose setup has been already completed, and the second one with large area Silicon α-ray detectors and a radiochemical section for thin α-samples preparation, whose setup is yet in progress and will be the argument of a separate work.The γ-ray spectrometer was calibrated by means of IAEA Reference Materials n. 312, 313, 314 and 375. A large difference from the predictions of secular equilibrium emerged between the activities of ²³⁴Th and ²³⁰Th in Materials n. 312, 313 and 314.     

博弈论在环境保护中的应用

阐述了博弈论的基本理论在环境保护中的应用,分析结果指出应结合市场机制和政府政策改变博弈方的收益,使博弈达到有利于环境保护的纳什均衡,提高环境保护效率;并探讨了博弈论在环境保护中应用的关键技术与策略。     

钙型斜发沸石铵离子交换平衡的研究

测定了在不同pH值下人工改型所得钙型斜发沸石对NH4^ 的全交换容量、对NH4^ 的等温交换平衡曲线，进一步研究了其部分热力学特性。结果表明，钙型斜发沸石对NH4^ 交换总量随pH值的升高而降低，在pH值为7时为79．321mmol／100g，该离子交换过程可自发进行，且其选择性随温度的升高而降低。研究成果可为沸石法处理含氨氮废水的进一步研究提供一定的理论依据。     

Characterization of primary precipitate composition formed during co-removal of Cr(VI) with Cu(II) in synthetic wastewater

BACKGROUND, AIMS AND SCOPE: Hexavalent chromium [Cr(VI)] cannot react with either carbonate or hydroxide to form chromium precipitates. However, by using a precipitation technology to treat plating wastewater containing Cr(VI), Cu(II), Ni(II) and Zn(II), approximately 78% of Cr(VI) (initial 60 mg/L) was co-removed with the precipitation of Cu(II), Ni(II) and Zn(II) (each 150 mg/L) by dosing with Na2CO3 (Sun 2003). Direct precipitation by forming Cu(II)-Cr(VI) precipitates followed by adsorption of Cr(VI) onto freshly formed Cu-precipitates was subsequently found to be the main mechanism(s) involved in Cr(VI) co-removal with Cu(II) precipitation by dosing Na2CO3 stepwise to various pH values (Sun et al. 2003). This study was. carried out to further characterize the formation of primary precipitates during the early stages of copper precipitation and simultaneous removal of Cr(VI) with Cu(II). METHODS: Test metal-solutions were prepared with industrial grade chemicals: CuCl2 x 2H2O, Na2SO4 and K2Cr2207. NaCO3 was added drop-wise to synthetic metal-solution to progressively increase pH. For each pH increment, removal of soluble metals was detected by atomic absorption spectrophotometer (AAS) and surface morphology of precipitates was analyzed by scanning electron microscope (SEM). To further characterize the formation of primary precipitates, a series of MINEQL+ thermodynamic calculations/analyses and equilibrium calculations/ analyses were conducted. RESULTS AND DISCUSSION: MINEQL+ thermodynamic calculation indicated that, for a system containing 150 mg/L Cu(II) and 60 mg/L Cr(VI) with gradual Na2CO3 dosing, if any precipitates can be formed at pH 5.0 or lower, it should be in the form of CuCrO4. Comparison tests using systems containing the same equivalent of Cu(II) plus Cr(VI) and Cu(II) plus SO4(2-) showed that the precipitation occurred at a pH of around 5.0 in the Cu(II)-Cr(VI) system and around 6.0 in the Cu(II)-SO4(2-) system. The discrepancy of the precipitation was indeed caused by the formation of Cu-Cr precipitates. The initiation of copper removal at pH around 5.0 for the Cu-Cr co-removal test was not attributable to the formation of Cu-CO3 precipitates, instead, it was most likely through the formation of insoluble Cu-Cr precipitates, such as CuCrO4 and CuCrO4 x 2Cu(OH)2. Experimental tests, equilibrium calculations, MINEQL+ thermodynamic calculations and surface morphologies for systems using higher concentrations of Cu(II) and Cr(VI) further verified the most probable composition of primary precipitates is copper-chromate. CONCLUSION: In the Cu-Cr co-removal test with Na2O3 dosing to increase pH and induce metal precipitation, copper-chromate precipitates are the primary precipitates produced and contribute to the initial simultaneous removal of copper and chromium.     

Comparision of China’s volatile organic compound pollution management: a computable general equilibrium approach

The public health and ecological impacts of volatile organic compound (VOCs) pollution have become a serious problem in China, arousing increasing attention to emissions control. In this context, this paper analyses the effectiveness of VOC reduction policies, namely pollution charges and environmental taxes at the national and industrial sector levels. It uses a computable general equilibrium model, which connects macroeconomic variables with VOC emissions inventory, to simulate the effects of policy scenarios (with 2007 as the reference year). This paper shows that VOC emissions are reduced by 2.2% when a pollution charge equal to the average cost of engineering reduction methods – the traditional approach to regulation in China – is applied. In order to achieve a similar reduction, an 8.9% indirect tax would have to be imposed. It concludes that an environmental tax should be the preferred method of VOC regulation due to its smaller footprint on the macroeconomy. Other policies, such as subsidies, should be used as supplements.     

雾霾期北京大气中多环芳烃污染特征及暴露风险评估

雾霾对我国尤其是华北平原地区造成了极大的困扰,其发生常以颗粒物浓度急剧增长为特征,给人群健康带来了极大的风险。为进一步阐释雾霾的形成过程及其健康效应,在冬季雾霾期对北京城区大气颗粒态及气态中18种多环芳烃(PAHs)进行了连续测定,同步监测颗粒物、痕量气体污染物以及气象参数的变化,并对PAHs的浓度、组成、气粒分配等大气行为以及其与气象因素的作用机制进行了探讨。北京城区大气气相和颗粒物相中ΣPAHs浓度分别为585 ng·m~(-3)和705 ng·m~(-3)。雾霾发生时,PM_(2.5)浓度升高了3.6倍,PAHs浓度升高了2.6倍,18种PAHs同系物的浓度均随PM_(2.5)的浓度线性增加,其线性相关性受PAHs来源以及氧化活性的影响;夜间较重质量数的PAHs相对比例增加,主要受日间交通源以及夜间燃烧源贡献强度影响。受颗粒物组成以及湿度的影响,雾霾天气下PAHs颗粒相分配率降低。进一步评估了北京城区人群的PAHs吸入健康效应,冬季雾霾频繁发生下其对人群癌症风险为6.2×10~(-5)。     

5种吸附剂对水中离子液体的吸附性能

实验研究了蒙脱土、活性白土、人造沸石、活性炭和水滑石5种吸附材料在25℃和50℃下对[Bmim]Cl的吸附过程,结果表明,蒙脱土对离子液体的去除效果最好,温度对活性炭的吸附有一定的影响,而对其他吸附剂的影响不大,说明这些无机矿物发生了离子交换型吸附过程。实验进一步研究了蒙脱土在25℃下对[Bmim]Cl、[Bmim]BF4、[Bmim]PF6、[Bmim]DBP、[Hmim]Cl和[Omim]Cl 6种离子液体的吸附行为,结果表明,对于阳离子相同的离子液体,阴离子对吸附影响不大;对于阴离子相同的离子液体,其饱和吸附量随着阳离子链长的增加而减小。