煤炭地下气化灰渣浸泡实验及Zn、Cd、Pb、As环境效应分析

为研究煤炭地下气化灰渣的环境效应,主要是对地下水的影响,以洛阳半焦煤为研究对象,进行煤炭地下气化的模型实验.取气化后的灰渣浸泡,测定浸出液中Zn、Cd、Pb和As4种元素的质量浓度.浸出液中Zn、Cd和As的质量浓度均低于地下水Ⅲ级标准.在饮用水允许的浓度范围内,不会对地下水造成多大污染;Pb的质量浓度在地下水Ⅴ类标准内,可能会对地下水造成一定污染.现场应考虑采取适当处理措施.4种元素的质量浓度均远低于浸出毒性鉴别标准值,因而不属于具有浸出毒性的危险废物.研究表明洛阳半焦煤地下气化灰渣中的Zn、Cd、Pb和As对环境的影响较小,不会对地下水产生多大影响.但在现场的工业试验中,由于长期的积累作用,也可能使元素的累积浓度超过地下水允许浓度,应定期监测.     

Dissipation and residue of triforine in strawberry and soil

Two independent field trials were performed in Guangdong and Hubei, China in 2011 to investigate the dissipation and residue levels of triforine in strawberry and soil. A fast and simple method using gas chromatography with electron capture detector was developed and validated to determine triforine levels in strawberry and soil. The average recovery of triforine in strawberry ranged from 87.46 to 104.32 % with a relative standard deviation (RSD) of 0.72 to 4.54 %; that in soil ranged from 83.82 to 103.01 % with an RSD of 3.89 to 4.36 %. The limit of quantification of the proposed method was 0.01 mg/kg for both strawberry and soil. The results suggest that the triforine dissipation curves followed the first-order kinetic. The half-lives of triforine in strawberry from Guangdong and Hubei were 3.58 and 4.42 days, respectively; those in soil were 3.53 and 4.10 days, respectively. The terminal residues of triforine in strawberry ranged from 0.032 to 0.264 mg/kg at preharvest intervals of 0.5, 1, and 3 days. These values are lower than the maximum residue limit of 1 mg/kg in strawberry set by the Codex Alimentarius Commission.     

The backend design of an environmental monitoring system upon real-time prediction of groundwater level fluctuation under the hillslope

The groundwater level represents a critical factor to evaluate hillside landslides. A monitoring system upon the real-time prediction platform with online analytical functions is important to forecast the groundwater level due to instantaneously monitored data when the heavy precipitation raises the groundwater level under the hillslope and causes instability. This study is to design the backend of an environmental monitoring system with efficient algorithms for machine learning and knowledge bank for the groundwater level fluctuation prediction. A Web-based platform upon the model-view controller-based architecture is established with technology of Web services and engineering data warehouse to support online analytical process and feedback risk assessment parameters for real-time prediction. The proposed system incorporates models of hydrological computation, machine learning, Web services, and online prediction to satisfy varieties of risk assessment requirements and approaches of hazard prevention. The rainfall data monitored from the potential landslide area at Lu-Shan, Nantou and Li-Shan, Taichung, in Taiwan, are applied to examine the system design.     

T酸一次洗水初步处理的研究

采用重氮化－偶合－混凝沉淀和重氮化－混凝沉淀两种方法对Ｔ酸一次洗水的初步处理进步了研究。Ｔ酸一次洗水经两种方法处理后,ＣＯＤ去除率分别为６１．３％、５０．５％,色度去除率分别为７４．６％、７１％。     

Polychlorinated biphenyls (PCBs) and halogenated flame retardants (HFRs) in multi-matrices from an electronic waste (e-waste) recycling site in Northern China

The present study investigated the occurrence of polychlorinated biphenyls (PCBs) and halogenated flame retardants (HFRs) in soil, water, reed, air and dust samples collected from the e-waste recycling region in Ziya Town, Northern China. The results showed that the concentrations of PCBs reached relative high level in environmental matrices in the study area. HFRs including polybrominated diphenyl ethers (PBDEs), dechlorane plus (DP), allyl 2,4,6-tribromophenyl ether (ATE), tetrabromoethylcyclohexane (TBECH), pentabromotoluene (PBT), pentabromoethylbenzene (PBEB), 2,3-dibromopropyl 2,4,6-tribromophenyl ether (DPTE), 1,2-bis-(2,4,6-tribromophenoxy) ethane (BTBPE) and so on were also widely detected in multi-matrices. Long-range atmospheric transport (LRAT) potentials of non-BDE HFRs were assessed to address the LRAR abilities of these compounds. Analysis of soil–air exchange of PCBs and HFRs showed that soil acted as a secondary source to the atmosphere only for a few low molecular weight compounds, while the direction of the flux of most detected chemicals was from air to soil.     

基于信息熵的省域内能源消费总量分配研究

能源消费总量控制是保障能源安全,积极应对气候变暖的重要手段;省域内能源消费量的合理分配,是落实国家能源消费总量控制的有效措施。提出能源消费总量分配应以公平为主、考虑区域发展权益的同时兼顾效率的原则,秉承“定基数,分增量”的思想,构建了基于信息熵的多因子混合加权分配模型,对目标年能源消费增量进行分配;选择了10个指标从经济水平、能耗水平、发展现状、产业结构及城市发展定位5个方面描述各地区的节能潜力及控制能耗量的责任,拟对能源消费总量在省内各市区的分配进行探索性研究。并以安徽省为例,对安徽省2015年能源消费总量分配到各市区进行了实证分析。结果显示,2015年安徽省17个市区能耗分配量增长率范围为1193%~5045%,能耗增幅的分配结果整体上受各市区人均GDP和人均能源消费量水平所支配,受单位工业增加值能耗和城市化率所调控     

Evaluating anthropogenic N inputs to diverse lake basins: A case study of three Chinese lakes

The environmental degradation of lakes in China has become increasingly serious over the last 30 years and eutrophication resulting from enhanced nutrient inputs is considered a top threat. In this study, a quasi-mass balance method, net anthropogenic N inputs (NANI), was introduced to assess the human influence on N input into three typical Chinese lake basins. The resultant NANI exceeded 10 000 kg N km⁻² year⁻¹ for all three basins, and mineral fertilizers were generally the largest sources. However, rapid urbanization and shrinking agricultural production capability may significantly increase N inputs from food and feed imports. Higher percentages of NANI were observed to be exported at urban river outlets, suggesting the acceleration of NANI transfer to rivers by urbanization. Over the last decade, the N inputs have declined in the basins dominated by the fertilizer use but have increased in the basins dominated by the food and feed import. In the foreseeable future, urban areas may arise as new hotspots for nitrogen in China while fertilizer use may decline in importance in areas of high population density.

Electronic supplementary material

The online version of this article (doi:10.1007/s13280-015-0638-8) contains supplementary material, which is available to authorized users.     

Influence of soil and hydrocarbon properties on the solvent extraction of high-concentration weathered petroleum from contaminated soils

Petroleum ether was used to extract petroleum hydrocarbons from soils collected from six oil fields with different history of exploratory and contamination. It was capable of fast removing 76–94 % of the total petroleum hydrocarbons including 25 alkanes (C₁₁–C₃₅) and 16 US EPA priority polycyclic aromatic hydrocarbons from soils at room temperature. The partial least squares analysis indicated that the solvent extraction efficiencies were positively correlated with soil organic matter, cation exchange capacity, moisture, pH, and sand content of soils, while negative effects were observed in the properties reflecting the molecular size (e.g., molecular weight and number of carbon atoms) and hydrophobicity (e.g., water solubility, octanol–water partition coefficient, soil organic carbon partition coefficient) of hydrocarbons. The high concentration of weathered crude oil at the order of 10⁵ mg kg^?1 in this study was demonstrated adverse for solvent extraction by providing an obvious nonaqueous phase liquid phase for hydrocarbon sinking and increasing the sequestration of soluble hydrocarbons in the insoluble oil fractions during weathering. A full picture of the mass distribution and transport mechanism of petroleum contaminants in soils will ultimately require a variety of studies to gain insights into the dynamic interactions between environmental indicator hydrocarbons and their host oil matrix.     

Historical change of mercury pollution in remote Yongle archipelago, South China Sea

We collected three ornithogenic coral sand sedimentary profiles from Jinyin Island, Jinqing Island and Guangjin Island of Yongle archipelago, South China Sea and reconstructed the deposition flux of anthropogenic Hg over the past 700 years in the study area. On the whole, the anthropogenic Hg flux is relatively low; it remained at a low level before the Industrial Revolution with a small peak at about 1450-1550 AD, which may record the enhanced metallurgy activity in Ming Dynasty of China. During the 20th century, the deposition flux of anthropogenic Hg increased rapidly, but two troughs occurred during the periods around 1940s and 1970s, corresponding to the economic depression caused by World War II, Civil War in China (1945-1949), and the Culture Revolution (1966-1976) in China. Since the 1970s the deposition flux of anthropogenic Hg has been persistently increasing, apparently the result of fast economic development in East and Southeast Asia countries around South China Sea.     

脱氮吸附剂深度脱除模拟含氮油中氮化物的研究

将磷钨酸、甲醛气体负载于介孔分子筛SBA-15中制备脱氮吸附剂,其中SBA-15、磷钨酸、甲醛的质量比为10∶7∶3.以喹啉、吲哚和咔唑为目标氮化物,二甲苯及二甲苯和十二烷的混合液为溶剂配制模拟含氮油,考察了反应温度、氮化物类型对脱氮反应速率的影响以及磷钨酸、甲醛的脱氮机制.结果表明,磷钨酸可以有效脱除碱性氮化物和低浓度非碱性氮化物,甲醛能强化吸附剂对非碱性氮化物的选择性.在70℃、脱氮吸附剂与高浓度模拟含氮油质量比为2.0∶30.0的条件下,模拟含氮油中的氮化物在90 min内可以被深度脱除.磷钨酸对碱性氮化物的脱除机制为磷钨酸和碱性氮化物间的配合作用和酸碱反应,磷钨酸对非碱性氮化物的脱除机制为氮化物和甲醛在酸催化下缩合反应生成聚合物.反应吸附剂再生回用后的脱氮能力随氮化物碱性的增强而减弱.