中国流域生态补偿标准核算方法分析

补偿标准核算是建立流域生态补偿机制的重要内容,也是生态补偿机制实施的关键环节.本文选取政策视角归纳了我国10个省份已经发布和实施的流域生态补偿政策的基本内容,对这些政策的补偿标准核算方法进行了分类,提出以成本和价值作为补偿标准核算方法分类的依据.结合流域生态补偿标准相关的研究成果以及国外政策,对我国流域生态补偿标准核算的政策内容进行了分析,在此基础上对政策层面流域生态补偿标准核算方法的发展和完善提出了建议.为了体现经济规律,同时增强生态补偿制度的激励作用,流域生态补偿政策中的补偿标准在污染赔偿方面需要进一步体现水污染造成的损失,在保护补偿方面需要体现水资源保护的经济价值.在未来我国流域生态补偿实施的过程中,相关方面协商确定补偿标准的趋势将会日益明显,在这个过程中各种量化核算和调查方法可以发挥比较重要的支持作用.本文的分析结果对于推动国家层面流域生态补偿标准核算政策制定或规范地方实践活动具有一定的参考价值.     

氚水在大豆土壤系统中的迁移与分布

采用模拟污染物的同位素示踪技术研究氚水在大豆-土壤模拟生态系统中的迁移、分布规律.通过为期50d的模拟试验,测定了植物和土壤样品中2种形态氚(自由水氚和结合态氚)的比活度.结果表明:引入土壤中的氚水,不仅在系统各分室间转移和分配,而且迅速向系统外散逸;氚水中的氚以自由水氚和结合态氚形态存在于大豆植株和土壤中;大豆植株中的自由水氚比活度于6h时即达最大值(根19.4Bq·g^-1;茎叶12.3Bq·g^-1),随后便逐渐下降,而结合态氚呈缓慢增加;大豆根中的总氚比活度开始时高于茎叶中的比活度,而后趋于平衡,表层土中2种形态氚基本呈逐渐下降.运用示踪动力学分室模型原理对实验数据拟合得:土壤中的比活度C_s=88.37e^-11.847t+7.38e^-0030t;大豆植株中的比活度C_b=10.30(e^-0.030t-e^-11.847t).     

介质阻挡放电等离子体直接分解NOx的影响因素

在以 γ- Al₂O₃小球作为填充物的介质阻挡放电条件下 ,研究放电电压 ( 9～ 16k V)、交流电源频率 ( 50～ 1600 Hz)、NO入口浓度 ( 50～1800 ml/m³)、气体空速 (1000～ 6500 h^-1)、反应温度 ( 20～250℃ )、介质小球比表面积及加入 O₂等因素对 NO分解率的影响 .发现提高放电电压、放电频率及介质小球比表面积能显著增加 NO分解率 ,O₂ 的加入对 NO的等离子体分解有强抑制作用 .     

水解-好氧系统处理生活污水的特性研究

采用新型 Yakult填料和中心导流式曝气方式 ,设计制作了新型生活污水净化装置 ,试验表明 ,停留时间 16 h左右 ,CODCr去除率 >80 % ,BOD5去除率 >90 % ,SS去除率 >85 % ,NH3 - N去除率 >87% ,出水水质达到国家一级排放标准     

Alkali resistance promotion of Ce-doped vanadium-titanic-based NH3-SCR catalysts

The effect of K deactivation on V_2O_5/WO_3-TiO_2 and Ce-doped V_2O_5/WO_3-TiO_2 catalysts in the selective catalytic reduction(SCR) of NOxby NH_3 was studied.Ce-doped V_2O_5/WO_3-TiO_2 showed significantly higher resistance to K deactivation than V_2O_5/WO_3-TiO_2.Ce-doped V_2O_5/WO_3-TiO_2 with K/V = 4(molar ratio) showed 90% NOxconversion at 350°C,whereas in this case V_2O_5/WO_3-TiO_2 showed no activity.The fresh and K-poisoned V_2O_5/WO_3-TiO_2 and Ce-doped V_2O_5/WO_3-TiO_2 catalysts were investigated by means of in situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS),NH_3-temperature progress decomposition(NH_3-TPD),X-ray photoelectron spectroscopy(XPS) and H2-temperature program reduction(H_2-TPR).The effect of Ce doping on the improving resistance to K of V_2O_5/WO_3-TiO_2 were discussed.     

浅海平台油气火灾事故模拟评估应用

全球海洋油气开发重特大火灾事故频发,油气生产安全面临严峻挑战,以我国浅海某中心平台组为研究对象,对可能发生的三相分离器喷射火火灾、管线交叉处喷射火火灾、生产平台池火火灾以及储罐平台池火火灾,采用FDS软件建立该平台组的火灾动力学模型,对油气泄漏后火灾的发展态势、火场温度、热辐射强度、设备温度以及不同火灾工况的对比分析,研究火灾发生后对人员伤害,以及平台上油气管线、分离器、油气储罐、平台栈桥等重要设备安全性的影响,并提出操作人员和重要设备的安全距离。针对火灾事故风险控制提出建议措施,对海上火灾风险分析未来研究方向进行阐述。     

Polymer hydrogels with enhanced stability and heterogeneous Fenton activity in organic pollutant removal

Polymer hydrogel-based materials have been shown to act as novel Fenton catalysts for water treatment, but the rational design of hydrogel-based catalysts with good stability has been a great challenge. To increase the stability and activity of polymer-based Fenton catalysts, uniform urchin-like α-Fe_2O_3 was grown in situ in a PVA carrier matrix here. PVA molecules promoted the growth of urchin-like α-Fe_2O_3, and then the PVA hydrogel acted as a barrier and carrier to reduce agglomeration. Through coordination by hydroxyl groups,PVA had good combination with Fe ions and α-Fe_2O_3. The formation of Fe–O–C bonds between iron oxides and polymers was reported for the first time, enhancing the material stability during catalysis. Under higher PVA concentrations, the resulting composite hydrogel could generate more ˙OH due to the increase in the number of active sites because of the hairy urchin-like structure. In tetracycline degradation through a heterogeneous Fenton reaction, the resulting material had good catalytic activity from pH 2 to pH 10 with low iron leaching, good reusability and remained at a level of nearly 90%after five consecutive cycles. Density functional theory calculations were used to further prove the mechanism of structural change of the iron oxides. The HOMO and LUMO energies of the iron oxides changed from 5.428 and 4.899 eV to 5.926 and 5.310 eV,indicating that the presence of PVA could influence the charge of the iron atom. The results provide new insights into the preparation of polymer hydrogel-based heterogeneous Fenton catalysts with enhanced stability for water treatment.     

Visible-light-driven photocatalytic inactivation of bacteriophage f2 by Cu-TiO2 nanofibers in the presence of humic acid

Pathogenic viruses in drinking water are great threats to public health. Visible-light-driven photocatalysis is a promising technology for virus inactivation. However, the existing photocatalytic antiviral research studies have mostly been carried out in single-component systems, neglecting the effect of natural organic matter, which exists widely in actual water bodies. In this paper, electrospun Cu-TiO₂ nanofibers were prepared as photocatalysts, and their photocatalytic antiviral performance in the presence of humic acid (HA) was comprehensively studied for the first time. The properties of the reaction mixture were measured during the reaction. In addition, the safety, reliability and stability of photocatalytic disinfection in the mixed system were evaluated. The results showed that the virus removal efficiency decreased with the increase of the HA concentration. The type of reaction solution, such as PBS buffer solution or water, did not affect the removal efficiency noticeably. Under acidic conditions, the electrostatic forces between photocatalysts and viruses were strengthened, leading to higher virus removal efficiency. As the reaction time went on, the pH value in the solution increased first and then tended to be stable, the conductivity remained stable, and the dissolved oxygen increased first and then decreased. The safety test showed that the concentration of Cu ions released into the solution was lower than specified by the international standards. No photoreactivation was observed, and the addition of HA significantly reduced the reutilization efficiency of the photocatalysts.     

Estimation and inter-comparison of dust aerosols based on MODIS, MISR and AERONET retrievals over Asian desert regions

This study presents detailed analysis of spatiotemporal variations and trend of dust optical properties i.e., Aerosol Optical Depth(AOD) and Angstrom component over Asian desert regions using thirteen years of data(i.e., 2001–2013) retrieved from Aerosol Robotic Network(AERONET), Moderate Resolution Imaging Spectroradiometer(MODIS) and Multi-angle Imaging Spectroradiometer(MISR). These regions include Solar Village, Dunhuang and Dalangzadgad and are considered as origin of desert aerosols in Asia. Mann–Kendall trend test was used to show the trend of AOD. The relationship of AOD with weather parameters and general AOD trend over different wavelengths has also been shown. AOD's trend has been observed significant throughout the year in Solar Village, while in Dunhuang and Dalanzadgad the significant trend has been found only in peak period(March–June).Analysis show high values of AOD and low values of angstrom in Solar Village during peak period. In Chinese desert regions, high values of AOD have been found during peak period and low values in pre-peak period. Significant relationship has been observed between AOD and average temperature in Solar Village and Dalanzadgad whereas rainfall and wind speed showed no significant impact on AOD in all desert regions.     

Enzyme-electrolytic degradation of dichloromethane: Efficiency, kinetics and mechanism

Enzymatic electrolysis cell(EEC) has advantages over microbial electrolysis cell(MEC) due to the needless of microbe inoculation and high-efficiency of enzymatic reaction. In this study, an EEC was first applied to achieve the effective degradation of halogenated organic pollutants and dichloromethane(CH_2Cl_2) was utilized as a model pollutant. The results indicate that the degradation efficiency of CH_2Cl_2 after 2 hr reaction in the EEC was almost100%, which was significantly higher than that with enzyme(51.1%) or current(19.0%). The current induced the continuous regeneration of reduced glutathione(GSH), thus CH_2Cl_2 was degraded under the catalysis of GSH-dependent dehalogenase through stepwise dechlorination, and successively formed monochloromethane(CH_3Cl) and methane(CH_4). The kinetic result shows that with a current of 15 mA, the maximum specific degradation rate of CH_2Cl_2(3.77 × 10~(-3) hr~(-1)) was increased by 5.7 times. The optimum condition for CH_2Cl_2 dechlorination was also obtained with pH, current and temperature of 7.0, 15 mA and 35°C,respectively. Importantly, this study helps to understand the behavior of enzymes and the fate of halogenated organic pollutants with EEC, providing a possible treatment technology for halogenated organic pollutants.