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71.
3种湿地填料对水体中氮磷的吸附特性研究 总被引:2,自引:0,他引:2
针对污染水体中氮磷超标问题,以海绵铁、沸石、砾石为填料,采用等温吸附、吸附动力学模型的方法开展3种湿地填料对氮磷吸附特性研究.结果表明:(1)填料对氮和磷的吸附均能用Langmuir和Freundlich方程描述.理论上对磷的吸附量依次为海绵铁>沸石>砾石;对氮依次为沸石>海绵铁>砾石.(2)双常数、一级动力学和Elovich方程动力学模型能够较好地描述填料对氮磷的等温吸附动力学特征,其中Elovich方程对3种填料的磷的吸附动力学特征描述更准确;一级动力学方程对沸石的氮的吸附动力学特征描述最精准.(3)填料对氮磷的吸附过程呈现先快后慢的整体趋势.从对氮磷的吸附量、吸附速率看,海绵铁和沸石能够作为人工湿地的填料对污水进行处理,并且经济方面较便宜,取用方便. 相似文献
72.
填埋场中亚硝酸还原酶测定条件的优化 总被引:1,自引:0,他引:1
填埋垃圾中的含氮化合物经一系列生物脱氮作用,最终使得填埋场中的氮素得以消减,在这一过程中亚硝酸还原酶起着十分重要的作用。以填埋场中的填埋垃圾为研究对象,在土壤亚硝酸还原酶测定方法的基础上,对亚硝酸还原酶活性测定条件进行了优化。结果表明,填埋垃圾中的亚硝酸还原酶活性测定的最优条件为:垃圾样品风干温度25℃,2mL的1%NaNO2溶液和2.5 mL的1%葡萄糖溶液,抽气5 min,置于25℃的培养箱中培养24 h。优化后的测定条件相对标准偏差(RSD)小于1.27%,表明该方法具有较高的灵敏度和精密度。 相似文献
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共代谢条件下丁基黄药的生物降解实验研究 总被引:5,自引:0,他引:5
微生物共代谢是降解废水中难降解有机物的重要方式。通过实验研究,比较了以丁基黄药作为唯一碳源和能源以及有共代谢基质存在下丁基黄药的降解过程。结果表明,共代谢显著提高了丁基黄药的降解率。在25℃条件下,以丁基黄药为唯一碳源和能源时,其降解率仅为43.1%;而利用葡萄糖作为共代谢基质,当葡萄糖质量浓度为0.20g/L时,振荡培养72h后丁基黄药的降解率可达65.2%;再加入微量的蛋白胨作为氮源后,丁基黄药的降解率可提高到73.5%;加入共代谢基质后微生物的适应期由原来的36h缩短至24h。共代谢是提高丁基黄药生物降解性能的一条有效途径。 相似文献
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Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in sediments of the Nansi Lake, China 总被引:2,自引:0,他引:2
Hong-Li Li Hong Gao Chen Zhu Guo-Gang Li Fan Yang Zheng-Yu Gong Jun Lian 《Environmental monitoring and assessment》2009,154(1-4):469-478
Polycyclic aromatic hydrocarbons (PAHs) were measured in surface sediments and dated core sediments from the Nansi Lake of China to investigate the spatial and temporal distribution characteristics. The concentrations of 16 kinds priority PAH compounds were determined by GC-MS method. And 210Pb isotope dating method was used to determine the chronological age of the sediment as well as the deposition rate. The results indicated that the total PAHs concentration ranges in surface and core sediment samples were 160 ~32,600 and 137 ~ 693 ng/g (dry wt.), respectively. The sediment rate and the average mass sedimentation were calculated to be 0.330 cm·year???1 and 0.237 g·cm???2·yr???1 and the sediment time of the collected core sample ranged from 1899 to 2000. The peak of PAH concentrations came at recent years. The source analysis showed PAHs mainly came from the contamination of low temperature pyrogenic processes, such as coal combustion. The PAHs concentrations were lower than ERL and LEL values for most collected samples. However, in several surface sediment samples especially in estuary sites, the PAHs concentrations were not only higher than ERL and LEL values, but also higher than ERM values. 相似文献
79.
The concentration levels, source, and inventories of polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) in 55 surface vegetable soils in the watershed of the Pearl River Delta (PRD) were analyzed and compared with those of the surface sediments in the Pearl River Estuary (PRE) and northern South China Sea (SCS). The 16 priority PAHs on US EPA list range from 58 to 3,077 microg/kg (average: 315 microg/kg). The concentrations of DDTs and HCHs range from 3.58 to 831 microg/kg (average: 82.1 microg/kg) and from 0.19 to 42.3 microg/kg (average: 4.42 microg/kg). The ratios of DDT/ (DDD+DDE) are higher than 2 in majority of the soil samples, suggesting that DDT contamination still exists. The PAH ratios suggest that the source of PAHs is petroleum, and combustion of fossil fuel, biomass, and coal. The average concentrations of PAHs and the linear regression slope between PAHs and TOC for the soils and the sediments are quite similar. It was estimated that the soil mass inventories at 0-20 cm depth are 1,292 metric tons for PAHs and 356 metric tons for OCPs in the studied region. The average PAHs inventory per unit area for the soil samples investigated in PRD is about 0.86 time that of surface sediments in the Pearl River Estuary, and about 2.43 times that of surface sediments in the northern South China Sea. PAHs in the soils in PRD have similar source to those of the surface sediments in PRE. All of those may suggest that PAHs in PRE and SCS are probably mainly inputted from the soils in PRD via soil erosion and river transport. 相似文献
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