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401.
本文以昌吉市为例,研究并分析了温度、风、气压三种自然因素对环境空气质量的影响.结果表明,影响环境空气质量的因素非常复杂,污染天气的形成与不利的自然气象因素密切相关.  相似文献   
402.
通过分析秦皇岛市2011—2012年每日的API值及大气PM10、 SO2、 NO2的日平均浓度变化与同时期的呼吸系统疾病日门诊人数资料,建立了时间序列分析数学模型,分析了秦皇岛市主要大气污染物与呼吸系统疾病发病的关系。发现秦皇岛市大气污染物的浓度与居民呼吸系统疾病之间存在着一定的正相关性,污染物浓度升高,居民呼吸系统疾病的就诊人数随之增加。  相似文献   
403.
气相色谱法测定室内空气中挥发性卤代烃   总被引:1,自引:0,他引:1  
建立了活性炭吸附-溶剂解吸-气相色谱测定室内空气中7种挥发性卤代烃的分析方法。样品经活性炭采样管富集后,用二硫化碳解吸,Agilent HP-1色谱柱分离,使用带有电子捕获检测器的气相色谱仪测定,以保留时间定性,外标法定量。当采样体积为10 L时,方法检出限范围是0.03~0.18 g/m3,加标回收率在72%~114%之间,相对标准偏差小于15%。结果表明,该方法可以应用于室内空气中痕量挥发性卤代烃样品的检测分析。  相似文献   
404.
目前烧结烟气脱硝主要采用活性炭(焦)吸附技术,投资及运行费用极高。SCR(选择性催化还原)烟气脱硝技术广泛应用于燃煤锅炉,技术成熟可靠。针对钢铁厂烧结烟气的特点,探讨了将SCR烟气脱硝技术应用于烧结烟气脱硝;通过适当的工艺优化和技术创新,烧结烟气采用SCR脱硝技术完全可行,经济适用。  相似文献   
405.
/ A number of strategies for the control of vehicular emissions are being considered by the Philippine government to address Metropolitan Manila's air quality problem. An analytical tool is needed for optimizing criteria pollutant reductions given the budgetary constraints. The simplest approach is to take costs and pollutant removals to be linear with each strategy's scale of activity, and this is readily solved as a linear programming problem. Another approach is to use a dynamic system of weights which shift with progressive improvements in pollutant emissions. The two approaches yield somewhat different results, suggesting the sensitivity of the solution to the assumed weights. The study also illustrates the importance of a sound methodology for evaluating priorities given to different air quality goals. One such methodology may involve a polling of expert panels and the public to gain insight into the relative importance given to competing emissions reduction goals. An informal polling of resource agency staff was conducted and discussed in this paper. The authors take the position that proper planning involves tracing intermediate steps to the final outcome and not just focusing on the latter.KEY WORDS: Vehicular emissions; Urban air quality; Emissions control; Optimization; Manila; Environmental systems analysis  相似文献   
406.
采集了4个市售飞灰螯合剂样品,分析其在20,40℃下挥发性污染物的释放规律.结果表明,释放的挥发性污染物主要有甲醛、乙醛、苯、异戊醛/异丙醇、甲硫醇、乙硫醇等;其中3个螯合剂样品甲醛的释放浓度在20℃为748~1325 μg/L-螯合剂,占释放的易挥发污染物的68%~96%(质量比),在40℃为4282~6822 μg/L-螯合剂,占释放的易挥发污染物的87%~95%(质量比).随着温度升高,释放的挥发性污染物种类变多,部分污染物浓度增加,40℃时,4个螯合剂样品释放的易挥发污染物浓度比20℃时增加了142%~444%.元素分析、拉曼光谱和热重分析结果表明,4个螯合剂的主要有效成分相似,为二硫代氨基甲酸盐类物质.因此,推测这种飞灰螯合剂在稀释和飞灰稳定化过程中,对工作人员的健康可能有潜在的危害风险,应收集释放的气体并进行处理;且在飞灰填埋过程中,可能会导致渗滤液中NH4+-N等物质的浓度升高,增加渗滤液的处理难度.  相似文献   
407.
我国居室内空气中甲醛污染现状分析及对策研究   总被引:4,自引:0,他引:4  
介绍了我国目前居室空气中甲醛污染现状,分析了居室空气中甲醛的来源及污染的成因。在实际工作中,摸索、总结了一套以在房间布局中设立衣帽间为核心的、防止因装修引起的居室空气中甲醛污染的具体办法。该办法简单、经济、适用面广,效果明显, 值得提倡和普及。  相似文献   
408.
A new air exchange rate (AER) monitoring method using continuous CO2 sensors was developed and validated through both laboratory experiments and field studies. Controlled laboratory simulation tests were conducted in a 1-m3 environmental chamber at different AERs (0.1-10.0 hr-1). AERs were determined using the decay method based on box model assumptions. Field tests were conducted in classrooms, dormitories, meeting rooms and apartments during 2-5 weekdays using CO2 sensors coupled with data loggers. Indoor temperature, relative humidity (RH), and CO2 concentrations were continuously monitored while outdoor parameters combined with on-site climate conditions were recorded. Statistical results indicated that good laboratory performance was achieved: duplicate precision was within 10%, and the measured AERs were 90%-120% of the real AERs. Average AERs were 1.22, 1.37, 1.10, 1.91 and 0.73 hr-1 in dormitories, air-conditioned classrooms, classrooms with an air circulation cooling system, reading rooms, and meeting rooms, respectively. In an elderly particulate matter exposure study, all the homes had AER values ranging from 0.29 to 3.46 hr??1 in fall, and 0.12 to 1.39 hr-1 in winter with a median AER of 1.15.  相似文献   
409.
An air pollution forecast system, ARIA Regional, was implemented in 2007-2008 at the Beijing Municipality Environmental Monitoring Center, providing daily forecast of main pollutant concentrations. The chemistry-transport model CHIMERE was coupled with the dust emission model MB95 for restituting dust storm events in springtime so as to improve forecast results. Dust storm events were sporadic but could be extremely intense and then control air quality indexes close to the source areas but also far in the Beijing area. A dust episode having occurred at the end of May 2008 was analyzed in this article, and its impact of particulate matter on the Chinese air pollution index (API) was evaluated. Following our estimation, about 23 Tg of dust were emitted from source areas in Mongolia and in the Inner Mongolia of China, transporting towards southeast. This episode of dust storm influenced a large part of North China and East China, and also South Korea. The model result was then evaluated using satellite observations and in situ data. The simulated daily concentrations of total suspended particulate at 6:00 UTC had a similar spatial pattern with respect to OMI satellite aerosol index. Temporal evolution of dust plume was evaluated by comparing dust aerosol optical depth (AOD) calculated from the simulations with AOD derived from MODIS satellite products. Finally, the comparison of reported Chinese API in Beijing with API calculated from the simulation including dust emissions had showed the significant improvement of the model results taking into account mineral dust correctly.  相似文献   
410.
The spatial concentrations, seasonal trends, profiles and congener pairs of ambient polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) were investigated within a seasonally active sampling scheme during Jun 2008 and Jan 2009 in Tianjin City, northern China. The PCDD/F concentrations ranged 14.2-172 fg I-TEQ/m3 (average 69.3 fg I-TEQ/m3) in summer and (89.8-1.01) × 103 fg I-TEQ/m3 (average 509 fg I-TEQ/m3) in winter, respectively, except for the E-waste dismantling site where much higher values were observed (1.04 × 103 fg I-TEQ/m3 in summer and 7.123 × 103 fg I-TEQ/m3 in winter). The results indicated a significantly seasonal trend with higher TEQ values in winter as compared with summer, which could be related to increased emission sources and seasonal variations of the atmospheric boundary layer height. 2,3,4,7,8-PeCDF was the dominant contributor to the total PCDD/F toxic equivalents, and 2,3,7,8-TCDD was detected at almost all the sampling sites in winter. Most of the similarly substituted PCDD/F congener pairs exhibited high correlations, suggesting that they might have similar environmental fate or sources. But different seasonal and spatial distributions of PCDD/F concentrations indicated that the emission sources might be intermittent.  相似文献   
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