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三峡库区规模化顺坡沟垄果园氮、磷输出过程及流失负荷 总被引:4,自引:0,他引:4
通过对三峡库区顺坡垄沟构型的规模化柑橘园集水区次降雨过程径流氮、磷进行动态监测,分析典型降雨事件氮和磷流失负荷,并探讨了规模化柑橘种植对土壤氮磷流失及入库河流水环境的影响.结果表明:①顺坡沟垄柑橘园集水区径流氮和磷年流失负荷分别为13.43 kg·(hm~2·a)~(-1)和1.26 kg·(hm~2·a)~(-1),春季施肥及强降雨冲刷是集水区污染物高负荷的主要原因;②集水区全年总氮(TN)和总磷(TP)的EMC为8.49 mg·L~(-1)和0.87 mg·L~(-1),超过发生水体富营养化含量标准;③春季施肥后的2场典型降雨中,长历时暴雨径流硝态氮(NN)和溶解态磷(DP)负荷为4.94 kg·hm~(-2)和0.28 kg·hm~(-2),分别占TN和TP流失负荷的92.90%和64.69%;短历时大雨径流NN和DP负荷为0.52 kg·hm~(-2)和0.05 kg·hm~(-2),分别占TN和TP的65.92%和74.88%,溶解态氮和磷是顺坡沟垄坡面果园径流氮和磷流失的主要途径;④集水区氮磷流失表现出显著的"初始冲刷效应",初期20%的地表径流流失了58.0%的TN, 57.0%的DN, 58.5%的NN, 79.0%的AN, 62.0%的TP, 63.5%的DP和60.0%的PP,控制初期地表径流对降低入库径流养分具有重要作用. 相似文献
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Extracellular polymeric substances (EPS) are organic metabolic compounds excreted by microorganisms. They largely impact microbial aggregate structures and functions. Extracellular polysaccharides (EP) in EPS are responsible for the formation of microbial aggregates. In this work, we successfully separated and characterized EP from EPS of the bacterium Bacillus megaterium TF10. Extraction of EP from EPS was optimized using Sevag''s reagent. Chemical characteristics, functional groups, and molecular weight (MW) distribu-tion of EP were compared with the harvested EPS and soluble microbial products (SMP). We found that the polymers of lower MW and free proteins were successfully removed by Sevag''s reagent. The higher MW components of EPS were predominantly polysaccharides, while the polymers of lower MW tended to secrete to the supernatant and were described as SMP. A part of the proteins in the EP was polysaccharide-bonded. Our results can be further used in elucidating the complex flocculation mechanisms in which EP play a major role. 相似文献
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Runmiao Xue Ariel Donovan Haiting Zhang Yinfa M Craig Adams John Yang Bin Hu Enos Inniss Todd Eichholz Honglan Shi 《环境科学学报(英文版)》2018,30(2):82-91
When adding sufficient chlorine to achieve breakpoint chlorination to source water containing high concentration of ammonia during drinking water treatment, high concentrations of disinfection by-products(DBPs) may form. If N-nitrosamine precursors are present, highly toxic N-nitrosamines, primarily N-nitrosodimethylamine(NDMA), may also form. Removing their precursors before disinfection should be a more effective way to minimize these DBPs formation. In this study, zeolites and activated carbon were examined for ammonia and N-nitrosamine precursor removal when incorporated into drinking water treatment processes.The test results indicate that Mordenite zeolite can remove ammonia and five of seven N-nitrosamine precursors efficiently by single step adsorption test. The practical applicability was evaluated by simulation of typical drinking water treatment processes using six-gang stirring system. The Mordenite zeolite was applied at the steps of lime softening, alum coagulation, and alum coagulation with powdered activated carbon(PAC) sorption. While the lime softening process resulted in poor zeolite performance, alum coagulation did not impact ammonia and N-nitrosamine precursor removal. During alum coagulation, more than67% ammonia and 70%–100% N-nitrosamine precursors were removed by Mordenite zeolite(except 3-(dimethylaminomethyl)indole(DMAI) and 4-dimethylaminoantipyrine(DMAP)). PAC effectively removed DMAI and DMAP when added during alum coagulation. A combination of the zeolite and PAC selected efficiently removed ammonia and all tested seven N-nitrosamine precursors(dimethylamine(DMA), ethylmethylamine(EMA), diethylamine(DEA), dipropylamine(DPA), trimethylamine(TMA), DMAP, and DMAI) during the alum coagulation process. 相似文献
516.
为有效控制白酒废水中高质量浓度NH4+-N对A/O系统冲击引起的出水水质超标问题,分析比较单级A/O工艺和分段进水两级A/O工艺[进水时间(以min计)分配比为7:3]对白酒废水的处理效果.结果表明:与单级A/O工艺相比,分段进水两级A/O工艺出水中ρ(NH4+-N)、ρ(NO2--N)、ρ(NO3--N)和ρ(CODCr)均显著降低,其平均去除率分别提高了16.9%、43.2%、49.7%和8%.分段进水两级A/O工艺的二次进水能够为短程硝化反硝化的进行提供有效碳源和NH4+-N等,为NO2--N和NO3--N等去除提供了有利条件;同时,它通过促进对系统内碳源的利用以及NO2--N的去除,进一步降低了出水中ρ(CODCr).此外,分段进水两级A/O工艺通过降低NH4+-N和NO2--N等污染物质量浓度,也能有效减弱其对氨氧化菌和亚硝酸盐氧化菌等微生物的抑制作用,为后续好氧阶段含氮污染物的去除奠定基础.但是,分段进水两级A/O工艺对白酒废水中PO43-的去除效果有限,这主要是因为第二阶段的NO2--N存在使反应系统处于缺氧环境,同时在碳源不充足的情况下,导致聚磷微生物释磷不充分,降低了第二好氧段的吸磷动力.研究显示,分段进水两级A/O工艺能够有效强化白酒废水中三态氮和CODCr的降解去除. 相似文献
517.
Yangtze River Delta(YRD) area is one of the important economic zones in China. However,this area faces increasing environmental problems. In this study, we use ground-based multi-axis differential optical absorption spectroscopy(MAX-DOAS) network in Eastern China to retrieve variations of NO_2, SO_2, and formaldehyde(HCHO) in the YRD area. Three cities of YRD(Hefei, Nanjing, and Shanghai) were selected for long-term observations. This paper presents technical performance and characteristics of instruments, their distribution in YRD, and results of vertical column densities(VCDs) and profiles of NO_2, SO_2, and HCHO.Average diurnal variations of tropospheric NO_2 and SO_2 in different seasons over the three stations yielded minimum values at noon or in the early afternoon, whereas tropospheric HCHO reached the maximum during midday hours. Slight reduction of the pollutants in weekends occurred in all the three sites. In general trace gas concentrations gradually reduced from Shanghai to Hefei. Tropospheric VCDs of NO_2, SO_2, and HCHO were compared with those from Ozone Monitoring Instrument(OMI) satellite observations, resulting in R~2 of 0.606, 0.5432, and 0.5566, respectively. According to analysis of regional transports of pollutants, pollution process happened in YRD under the north wind with the pollution dissipating in the southeast wind. The feature is significant in exploring transport of tropospheric trace gas pollution in YRD, and provides basis for satellite and model validation. 相似文献
518.
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. 相似文献
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