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1.
城市污水污泥焚烧过程中的重金属迁移特性   总被引:25,自引:0,他引:25  
重金属是污泥对环境污染的一个重要方面,实验证明,焚烧是防止重金属污染的优选处理方法。通过分析重金属元素在污泥中的存在形式及对高碑店污水理处厂污泥焚烧前后重金属含量的变化进行检测,研究了重金属在焚烧处理过程中迁移特性。结果表明,重金属在焚烧过程中迁移特性因其种类和燃烧工况而不同。根据研究结果,提出了污泥灰渣处理的建议。  相似文献   
2.
应用地质累积指数评价攀枝花地区土壤重金属污染   总被引:46,自引:0,他引:46  
应用地质累积指数对攀枝花地区昔格达组粘土中重金属污染进行了评价研究。结果表明,各重金属元素污染较严重的地区分布在宝顶煤矿、太平煤矿、攀钢冶钢厂、攀钢矿山、尾矿坝等工矿区,污染较轻微的地区分布在红格、新九等农业区。各元素的污染程度上看,该区As和Cu污染较重,Cd,Pb,Zn次之,而Cr污染最轻微。  相似文献   
3.
以宁夏吴忠市金积傍河水源地为研究对象,在综合分析水源地区内土壤介质特征基础上,在水源地区域范围内采集了15个土壤样品,分析了区域范围内土壤重金属砷、镉、铬、铜、铅、镍、锰等7个因子空间分布状况,采用正定矩阵分析方法定性识别土壤重金属来源及各项来源空间污染贡献率。结果显示,金积水源地土壤重金属含量均未超过国家土壤环境二级标准,低于区域土壤背景值,其中土壤重金属污染受自然来源总贡献率为34.1%,受工业污染影响来源贡献率26.2%,受农业污染影响来源贡献率21.1%,受畜禽养殖粪便堆放及施肥作用影响的贡献率为18.6%。污染来源及其污染贡献程度分析结果为水源地供水安全和环境保护提供了重要的科学依据。  相似文献   
4.
化石燃料原油和原煤的燃烧、含钒矿石的开采和冶炼是大气中重金属钒的主要来源。文章利用重金属钒的排放系数分析了中国1978-2010年人为过程释放到大气中重金属钒的总量和行业重金属钒的排放,预测了2020年和2030年中国大气中重金属钒的排放量。结果表明,自1978年以来,中国钒的排放量增加了4倍,中国2010年人类活动向大气排放的重金属钒总量达3.18万吨,约占世界总量的12%。原油燃烧释放到大气中的钒约占总量的85%,煤炭燃烧的排放量占10.5%,其中工业耗油向大气中释放重金属钒的比例从1980的71%下降到2008年的42%,总量从3 721 t增加至9 361 t;交通运输行业从10%上升到36%,总量从547 t增加至7 967 t;其它行业(农林牧渔水利业、批发零售业和住宿餐饮业、生活消费)基本维持在20%左右,总量从986 t增加至5 052 t。因此,应加强大气中钒的监测和管理,预防大气钒污染事件的发生。  相似文献   
5.
In order to measure groundwater age and design nuclear waste disposal sites, it is important to understand the sorption behavior of tritium on soils. In this study, batch tests were carried out using four soils from China: silty clays from An County and Jiangyou County in Sichuan Province, both of which could be considered candidate sites for Very Low Level Waste disposal; silty sand from Beijing; and loess from Yuci County in Shanxi Province, a typical Chinese loess region. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. The average distribution coefficient from all of these influencing factors was about 0.1-0.2 mL/g for the four types of soil samples. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment.  相似文献   
6.
In order to investigate the distribution of the total petroleum hydrocarbons (TPH) in groundwater and soil, a total of 71 groundwater samples (26 unconfined groundwater samples, 37 confined groundwater samples, and 8 deeper confined groundwater samples) and 80 soil samples were collected in the Songyuan oilfield, Northeast China, and the vertical variation and spatial variability of TPH in groundwater and soil were assessed. For the groundwater from the unconfined aquifer, petroleum hydrocarbons were not detected in three samples, and for the other 23 samples, concentrations were in the range 0.01–1.74 mg/l. In the groundwater from the confined aquifer, petroleum hydrocarbons were not detected in two samples, and in the other 35 samples, the concentrations were 0.04–0.82 mg/l. The TPH concentration in unconfined aquifer may be influenced by polluted surface water and polluted soil; for confined aquifer, the injection wells leakage and left open hole wells may be mainly responsible for the pollution. For soils, the concentrations of TPH varied with sampling depth and were 0–15 cm (average concentration, 0.63 mg/g), >40–55 cm (average concentration, 0.36 mg/g), >100–115 cm (average concentration, 0.29 mg/g), and >500–515 cm (average concentration, 0.26 mg/g). The results showed that oil spillage and losses were possibly the main sources of TPH in soil. The consequences concluded here suggested that counter measures such as remediation and long-term monitoring should be commenced in the near future, and effective measures should be taken to assure that the oilfields area would not be a threat to human health.  相似文献   
7.
通过静态吸附实验,探究凹凸棒石黏土对四环素和土霉素的吸附动力学;采用准一级动力学、准二级动力学和颗粒内扩散模型拟合实验数据,分析吸附过程。测定凹凸棒石黏土对四环素和土霉素的动态吸附曲线和吸附容量,研究凹凸棒石黏土对水溶液中四环素和土霉素的动态吸附性能。探讨初始质量浓度对穿透曲线的影响,采用Thomas模型对动态试验数据拟合,获得相关参数。结果表明,凹凸棒石黏土能够有效去除水中的四环素和土霉素,且四环素的吸附容量高于土霉素,在初始浓度为400mg/L时,对四环素的饱和吸附量达74.5mg/g,对土霉素的饱和吸附量达69.2mg/g。穿透曲线呈S型,且随着初始浓度的增大,穿透点向左移,穿透时间缩短,平衡吸附量增加。  相似文献   
8.
将环境示踪技术用于地下水定年以确定地下水的相关时间尺度问题在过去几十年中得到了长足发展,尤其是在年轻地下水定年方面。目前国内外用到的年轻地下水环境示踪剂有多种,这些示踪剂在地下水定年方面各有利弊。本文的目的是对国内外现有的9种年轻地下水示踪剂(3 H、3 H/3 He、4 He、35S、36 Cl/Cl、85 Kr、222 Rn、CFCs和SF6)的来源、示踪原理、误差来源、优缺点、适用性和应用现状等进行归纳和总结,为研究者、管理者和决策者在应用时提供参考。  相似文献   
9.
The nonpoint source (NPS) pollution is difficult to manage and control due to its complicated generation and formation. Load estimation and source apportionment are an important and necessary process for efficient NPS control. Here, an integrated application of semi-distributed land use-based runoff process (SLURP) model, export coefficients model (ECM), and revise universal soil loss equation (RUSLE) for the load estimation and source apportionment of nitrogen and phosphorus was proposed. The Jinjiang River (China) was chosen for the evaluation of the method proposed here. The chosen watershed was divided into 27 subbasins. After which, the SLURP model was used to calculate land use runoff and to estimate loads of dissolved nitrogen and phosphorus, and ECM was applied to estimate dissolved loads from livestock and rural domestic sewage. Next, the RUSLE was employed for load estimation of adsorbed nitrogen and phosphorus. The results showed that the 12,029.06 t?a?1 pollution loads of total NPS nitrogen (TN) mainly originated from dissolved nitrogen (96.24 %). The major sources of TN were land use runoff, which accounted for 45.97 % of the total, followed by livestock (32.43 %) and rural domestic sewage (17.83 %). For total NPS phosphorous (TP), its pollution loads were 570.82 t?a?1 and made up of dissolved and adsorbed phosphorous with 66.29 and 33.71 % respectively. Soil erosion, land use runoff, rural domestic sewage, and livestock were the main sources of phosphorus with contribution ratios of 33.71, 45.73, 14.32, and 6.24 % respectively. Therefore, land use runoff, livestock, and soil erosion were identified as the main pollution sources to influence loads of NPS nitrogen and phosphorus in the Jinjiang River and should be controlled first. The method developed here provided a helpful guideline for conducting NPS pollution management in similar watershed.  相似文献   
10.
采用微波炉对一定质量的氢氧化钙样品进行活化,利用压汞仪考察了不同微波活化时间及脱氯反应前后的Ca(OH)2总比孔表面积、分段比表面积和孔径分布的变化,并在脱氯实验台上对脱氯效率进行实际测试。结果表明,微波活化存在一个最佳时间,在此时间内样品比孔表面积增大50%左右,而超过这一时间样品比表面积回复性减小;微波活化主要通过增加3~20 nm孔径段的微孔为样品提供更大比表面积;这些新增加的微孔在脱氯反应过程中被完全利用或消耗; 最佳活化时间下的微波活化使Ca(OH)2在较低Ca/Cl摩尔比下获得更大脱氯效率,Ca/Cl摩尔比=4.1时,脱氯效率增加了20%。  相似文献   
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