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621.
膜生物反应器无剩余污泥排放的研究 总被引:42,自引:2,他引:40
本文介绍了以膜生物反应器为基础的剩余污泥产量最少或无剩余污泥产生的最新的污水处理理论和技术。从技术微生物基本生命活动的物质转化概念和细胞产生和平衡的理论,提出了确定维持微生物基本生命活动的物质转化系数的方法,从理论与实验上计实了膜生物反应器无剩余污泥排放的可能性。 相似文献
622.
Chen Xuemin Wu Weifeng Liu Yun Liu Chenrui Tian Jiang Li Feng Dang Zhi 《Environmental Chemistry Letters》2023,21(6):3077-3082
Environmental Chemistry Letters - Acid mine drainage is highly acidic and contains heavy metals, which can be harmful to soil, water, plants, and animals. To solve this issue, surface passivation... 相似文献
623.
Yuting Wei Xiao Tian Junbo Huang Zaihua Wang Bo Huang Jinxing Liu Jie Gao Danni Liang Haofei Yu Yinchang Feng Guoliang Shi 《Frontiers of Environmental Science & Engineering》2023,17(11):137
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具有抗菌功能的生物防护口罩对于预防呼吸道传染病的流行、保护人员健康具有重要的意义。本文采用化学键结合的方法将生物抗菌剂ε-聚赖氨酸(ε-PL)固定在聚对苯二甲酸乙二酯(PET)非织造布上并与其它过滤材料复合,采用密合拱型结构设计研制出一种具有抗菌功能的生物防护口罩。实验结果表明,该口罩对菌悬液和微生物气溶胶的抗菌率分别为99.99%和81.9%,且抗菌性能稳定;对颗粒气溶胶和微生物气溶胶的过滤效率分别为99.32%和99.99%,在满足GB19083的基础上具有优良的生物防护性能。 相似文献
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Biosolids are known to have a potential to restore degraded land, but the long-term impacts of this practice on the environment, including water quality, still need to be evaluated. The surface water chemistry (NO3-, NH4+, and total P, Cd, Cu, and Hg) was monitored for 31 yr from 1972 to 2002 in a 6000-ha watershed at Fulton County, Illinois, where the Metropolitan Water Reclamation District of Greater Chicago was restoring the productivity of strip-mined land using biosolids. The mean cumulative loading rates during the past 31 yr were 875 dry Mg ha(-1) for 1120-ha fields in the biosolids-amended watershed and 4.3 dry Mg ha(-1) for the 670-ha fields in the control watershed. Biosolids were injected into mine spoil fields as liquid fertilizer from 1972 to 1985, and incorporated as dewatered cake from 1980 to 1996 and air-dried solids from 1987 to 2002. The mean annual loadings of nutrients and trace elements from biosolids in 1 ha were 735 kg N, 530 kg P, 4.5 kg Cd, 30.7 kg Cu, and 0.11 kg Hg in the fields of the biosolids-amended watershed, and negligible in the fields of the control watershed. Sampling of surface water was conducted monthly in the 1970s, and three times per year in the 1980s and 1990s. The water samples were collected from 12 reservoirs and 2 creeks receiving drainage from the fields in the control watershed, and 8 reservoirs and 4 creeks associated with the fields in the biosolids-amended watershed for the analysis of NO3- -N (including NO2- N), NH4+-N, and total P, Cd, Cu, and Hg. Compared to the control (0.18 mg L(-1)), surface water NO3- -N in the biosolids-amended watershed (2.23 mg L(-1)) was consistently higher; however, it was still below the Illinois limit of 10 mg L(-1) for public and food-processing water supplies. Biosolids applications had a significant effect on mean concentrations of ammonium N (0.11 mg L(-1) for control and 0.24 mg L(-1) for biosolids) and total P (0.10 mg L(-1) for control and 0.16 mg L(-1) for biosolids) in surface water. Application of biosolids did not increase the concentrations of Cd and Hg in surface water. The elevation of Cu in surface water with biosolids application only occurred in some years of the first decade, when land-applied sludges contained high concentrations of trace metals, including Cu. In fact, following the promulgation of 40 CFR Part 503, the concentrations of all three metals fell below the method detection level (MDL) in surface water for nearly all samplings. Nitrate in the surface water tends to be higher in spring, and ammonium, total P, and total Hg in summer and fall. Mean nitrate, ammonium, and total phosphorus concentrations were found to be greater in creeks than reservoirs. The results indicate that application of biosolids for land reclamation at high loading rates from 1972 to 2002, with adequate runoff and soil erosion control, had only a minor impact on surface water quality. 相似文献
629.
微波辐射在二氧化锰诱导下对六氯苯污染土壤的修复研究 总被引:4,自引:0,他引:4
以二氧化锰为微波吸附剂,在密封体系中研究了微波辐射技术对六氯苯污染土壤的修复效果。分别以不同浓度的酸碱水溶液添加到土壤中,在模拟含水率为20%情况下,硫酸(50%)介质下六氯苯处理效果最好,10min的微波辐射即可使50mg/kg的六氯苯达到完全去除;但是在纯水和10mol/L氢氧化钠介质下,六氯苯基本上没有去除;随着硫酸浓度的降低,六氯苯的去除率显著降低。气相色谱/质谱联用(GC/MS)分析没有检测到新物质。六氯苯去除机理推测为,直接矿化或者HCB及其分解的中间产物同土壤发生化学结合而被固定起来,以致难以萃取出来。 相似文献
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