Effects of leachate accumulation on landfill stability in humid regions of China

Leachate levels are important to landfill stability and safety. High leachate or water levels often lead to landfill instability, which can cause accidents. Here a case study of a landfill located in a humid region of southern China is presented. Leachate distribution and quality were systematically analyzed, and the effect of leachate level on waste-mass stability was assessed. Boreholes were drilled in the field, samples were analyzed in the laboratory, and a simulation was performed. In addition, the safety and stability of the landfill was evaluated. The leachate level in the landfill was 9–19 m, which was higher than the top of the dam crest (8–20 m). Leachate accounted for more than 1/4 of the total landfill storage capacity. The contaminant concentration of the leachate samples collected directly from the waste body was very high, with large variation among the samples. The mean concentrations of NH₃–N, BOD, and COD from the waste body were 5404, 14,136, and 22,691 mg/L, nearly 2.7, 2.4, and 1.8 times the mean concentrations in the leachate pond, respectively. Three series of shear strength parameters were used in a slope stability analysis, and a limit equilibrium method was used to calculate the factor of safety (Fs). The analysis showed that Fs could be affected by potential anisotropy in the shear strength of the waste. The minimum values of Fs corresponding to series I were 1.84 and 1.17 for units ? and II, respectively. The Fs value of unit II was significantly lower than the safe design value (1.25). In addition, Fs decreased with increase in the normalized height of the leachate level, h/H, where h is the height of the leachate mound and H is the maximum thickness of the landfill. If the h/H values of units I and II are kept below 50% and 40%, respectively, a safe design value of 1.25 for Fs can be guaranteed. Therefore, some measures to prevent risk should be considered.     

Study of nitrogen oxide absorption in the calcium sulfite slurry

Experiments were conducted using a bubbling reactor to investigate nitrogen oxide absorption in the calcium sulfite slurry. The effects of CaSO₃ concentration, NO₂/NO mole ratio and O₂ concentrations on NO₂ and SO₂ absorption efficiencies were investigated. Five types of additives, including MgSO₄, Na₂SO₄, FeSO₄, MgSO₄/Na₂SO₄ and FeSO₄/Na₂SO₄, had been evaluated for enhancing NO₂ absorption in CaSO₃ slurry. Results showed that CaSO₃ concentration had significant impact on NO₂ and SO₂ absorption efficiencies, and the highest absorption efficiencies of SO₂ and NO₂ could reach about 99.5 and 75.0 %, respectively. Furthermore, the NO₂ absorption was closely related to the NO₂/NO mole ratio, and the existence of NO₂ in flue gas may promote NO absorption. The presence of O₂ in simulated flue gas was disadvantage for NO _x removal because it can oxidize sulfite to sulfate. It was worth pointing out that FeSO₄/Na₂SO₄ was the best additive among those investigated additives, as the NO₂ removal efficiency was significantly increased from 74.8 to 95.0 %. IC and in situ FTIR results suggest that the main products were NO₃ ^? and NO₂ ^? in liquid phase and N₂O, N₂O₅ and HNO₃ in gas phase during the CaSO₃ absorption process.     

构建“水-煤-碳”体系 优化煤化工发展

分析了煤化工行业发展的现状及趋势,提出我国现代煤化工发展瓶颈主要是产业发展存在技术风险、产业发展与资源环境的矛盾突出及面临碳减排压力,并提出通过合理构建"水-煤-碳"三大约束指标体系,引导煤化工实现有序发展。     

ClO2氧化法预处理联苯胺类染料中间体废水

采用ClO₂氧化法预处理联苯胺类染料中间体生产废水,探讨了影响COD和联苯胺去除率的主要因素,并采用GC/MS技术对ClO₂氧化前后废水中的有机组分进行了分析。实验确定了较佳的工艺参数：ClO₂加入量为45~55 mg/L,ClO₂与联苯胺的化学计量比控制在（3.0~3.5）∶1,反应时间为 30~35 min。在此条件下,ClO₂氧化后出水中联苯胺去除率达到80%以上,联苯胺类污染物含量得到有效降低,废水BOD₅/COD由原水的0.18提高到0.40。该方法能提高废水的可生化性,是一种较好的生化预处理技术。     

Characterization of Dust Storms to Hong Kong in April 1998

In April 1998, two intense dust storms were generated in CentralAsia and transported eastward across East Asia (15 and 19 April). This article presents the chemical characterization ofHong Kong (HK) aerosols during the dust storms. During the 15 Aprildust storm, hourly respiratory suspended particles (RSP)(particle diameter smaller than 10 m) concentrationsmonitored at 7 sites in Hong Kong reached the peak valuessynchronously between 9 and 11 a.m. on 17 April, in which thehighest concentration was 267 g m^-3. Analysis ofthe RSP samples showed that concentrations of crustalelements (Ba, Ca, Cd, Cr, Fe, Mg, K⁺) and anthropogenicspecies (As, Ni, Pb, Zn, NH₄ ⁺, NO₃ ^-,SO₄ ^2- and total carbon) were substantiallyenhanced. Enhancement of these species was more than afactor of 2 to 14 relative to the non dust period. The totalcarbon content was high, at 59 g m^-3 (notincluding carbonate), and the enrichment factors of Asand Pb on 17 April were 122 and 117, respectively. Thisimplied that anthropogenic materials together with mineraldust were transported to HK from Mainland China. Based onmaterial balance calculations, mineral dust contributed41% to the observed RSP mass on 17 April, which was 2 times thatof the nondust sample (22%). From the 5-day backwardtrajectory analysis, this storm was transported directlyfrom Northwest China to HK. However, there was nocorresponding observation for the 19 April dust stormaerosol. Consequently, 15 April storm had stronger impact onHK's atmosphere than 19 April storm. Compared to the HK AirQuality Objective, 15 April dust storm did not cause seriousair pollution in HK.     

An overview on the processes and technologies for recycling cathodic active materials from spent lithium-ion batteries

This paper aims to make an overview on the current status and new tendency for recycling cathodic active materials from spent lithium-ion batteries. Firstly, it introduces several kinds of pretreatment technologies, followed by the summary of all kinds of single recycling processes mainly focusing on organic acid leaching and synergistic extraction. Then, several examples of typical combined processes and industrial recycling processes are presented in detail. Meanwhile, the advantages, disadvantages and prospect of each single process, combined process, as well as industrial recycling processes, are discussed. Finally, based on a novel acidic organic solvent, the authors briefly introduce an environmental friendly process to directly recycle and resynthesize cathodic active material LiNi_1/3Co_1/3Mn_1/3O₂ from spent lithium-ion batteries. The preliminary experimental results demonstrated the advantages of low reaction temperature, high separation efficiency and organic solvent cycling and preventing secondary pollution to the environment. This process may be used for large-scale recycling of spent lithium-ion batteries after further study.     

粉煤灰的改性及对刚果红的吸附

分别采用沸水浸泡、酸浸、碱浸和加热的方法对粉煤灰进行改性处理,利用FTIR仪和XRD仪对改性粉煤灰的成分和官能团进行了分析,并利用改性粉煤灰对模拟刚果红废水进行脱色。实验结果表明：碱改性粉煤灰中含有大量官能团,以及NaPl型沸石类物质,能够明显提高粉煤灰对刚果红的吸附性能;与活性炭相比,碱改性粉煤灰具有更高的性价比;在初始刚果红质量浓度为20mg/L、碱改性粉煤灰加入量为50g/L的条件下,废水的脱色率可达87.52%;碱改性粉煤灰对刚果红的吸附过程遵循二级反应动力学,较好地符合Langmuir等温式和Freundlich等温式。     

新民居建设中农村环境教育的发展思路

新民居建设是建设社会主义新农村的重要举措,发展农村环境教育能有效促进农村环境的改善。我国农村环境教育目前存在重视程度不够、教育主体和方式相对单一以及缺乏必要的教育目标等问题。在发展农村环境教育方面明确受教育的主体,并从扩大教育实施主体、开展直接教育和间接教育以及增加政府财经投入等方面入手,才能实现经济发展与农村环境改善的协调发展。     

生态移民安置区耕地景观生态安全评价——以宁夏红寺堡为例

利用1995年、2005年和2015年三个时期遥感影像,对研究区耕地景观生态安全进行综合评价,分析了移民安置区耕地景观生态安全特征及其驱动因素。结果表明:移民安置区的耕地景观生态安全呈下降趋势。安置区耕地景观生态安全格局也在变化,1995—2005年Ⅱ级区有向Ⅲ级区转化,2005—2015年Ⅰ级区和Ⅲ级区都向Ⅱ级区转化。土地利用政策、生态移民及人口增长是耕地景观生态安全变化主要驱动因素。     

Modeling the fate of benzo[a]pyrene in the wastewater-irrigated areas of Tianjin with a fugacity model

A Level III fugacity model was applied to characterize the transfer processes and environmental fate of benzo[a]pyrene in wastewater-irrigated areas of Tianjin, China. The physical-chemical properties and transfer parameters of benzo[a]pyrene were used in the model and the concentration distribution of benzo[a]pyrene in sediment, soil, water, air, fish, and crop compartments, as well as transfer fluxes across the compartments, were then derived under steady-state assumptions. The calculated results were compared with monitoring data for air, soil, water, and sediment collected from the literature. The results indicate that there was generally good agreement and the differences were within an order of magnitude for air, soil, and sediment. The concentration of benzo[a]pyrene in the ambient air in the area was very low with a majority present sorbed to aerosol. In the water compartment, approximately 70% of benzo[a]pyrene dissolved in water phase. Relatively high concentrations of the compound were found in the soil and sediment, with the soil serving as the dominant sink in the area. Benzo[a]pyrene, with a slow metabolic rate, was found to accumulate in fish in the area.