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91.
臭氧氧化—包埋菌流化床生物处理组合工艺深度处理煤气化废水 总被引:1,自引:0,他引:1
采用臭氧氧化—包埋菌流化床生物处理组合工艺对煤气化废水进行深度处理。实验结果表明:当臭氧的质量浓度20 mg/L、臭氧进气流量1.5 L/min、臭氧通气时间30 min、包埋菌流化床水力停留时间24 h时,臭氧氧化工序的COD去除率达到30.0%~40.0%,总酚去除率达到100.0%;包埋菌流化床工序的COD去除率达到60.0%以上,氨氮的去除率大于95.0%;经组合工艺处理后,出水COD<60 mg/L,ρ(氨氮)<1.0 mg/L,ρ(总酚)未检出,色度小于50倍,达到GB8978—1996《污水综合排放标准》中的一级排放标准。 相似文献
92.
Ye Sun Yuan Meng Xiaoyan Guo Tianle Zhu Hongju Liu Wenpei Li 《Journal of Material Cycles and Waste Management》2016,18(4):618-624
Experiments were conducted using a bubbling reactor to investigate nitrogen oxide absorption in the calcium sulfite slurry. The effects of CaSO3 concentration, NO2/NO mole ratio and O2 concentrations on NO2 and SO2 absorption efficiencies were investigated. Five types of additives, including MgSO4, Na2SO4, FeSO4, MgSO4/Na2SO4 and FeSO4/Na2SO4, had been evaluated for enhancing NO2 absorption in CaSO3 slurry. Results showed that CaSO3 concentration had significant impact on NO2 and SO2 absorption efficiencies, and the highest absorption efficiencies of SO2 and NO2 could reach about 99.5 and 75.0 %, respectively. Furthermore, the NO2 absorption was closely related to the NO2/NO mole ratio, and the existence of NO2 in flue gas may promote NO absorption. The presence of O2 in simulated flue gas was disadvantage for NO x removal because it can oxidize sulfite to sulfate. It was worth pointing out that FeSO4/Na2SO4 was the best additive among those investigated additives, as the NO2 removal efficiency was significantly increased from 74.8 to 95.0 %. IC and in situ FTIR results suggest that the main products were NO3 ? and NO2 ? in liquid phase and N2O, N2O5 and HNO3 in gas phase during the CaSO3 absorption process. 相似文献
93.
94.
Danny Reible David Lampert David Constant Robert D. Mutch Jr. Yuewei Zhu 《补救:环境净化治理成本、技术与工艺杂志》2006,17(1):39-53
An active capping demonstration project in Washington, D.C., is testing the ability to place sequestering agents on contaminated sediments using conventional equipment and evaluating their subsequent effectiveness relative to conventional passive sand sediment caps. Selected active capping materials include: (1) AquaBlokTM, a clay material for permeability control; (2) apatite, a phosphate mineral for metals control; (3) coke, an organic sequestration agent; and (4) sand material for a control cap. All of the materials, except coke, were placed in 8,000‐ft test plots by a conventional clamshell method during March and April 2004. Coke was placed as a 1.25‐cm layer in a laminated mat due to concerns related to settling of the material. Postcap sampling and analysis were conducted during the first, sixth, and eighteenth months after placement. Although postcap sampling is expected to continue for at least an additional 24 months, this article summarizes the results of the demonstration project and postcap sampling efforts up to 18 months. Conventional clamshell placement was found to be effective for placing relatively thin (six‐inch) layers of active material. The viability of placing high‐value or difficult‐to‐place material in a controlled manner was successfully demonstrated with the laminated mat. Postcap monitoring indicates that all cap materials effectively isolated contaminants, but it is not yet possible to differentiate between conventional sand and active cap layer performance. Monitoring of the permeability control layer indicated effective reductions in groundwater seepage rates through the cap, but also showed the potential for gas accumulation and irregular release. All of the cap materials show deposition of new contaminated sediment onto the surface of the caps, illustrating the importance of source control in maintaining sediment quality. © 2006 Wiley Periodicals, Inc. 相似文献
95.
96.
The effect of ammonia inhibition was evaluated during the enhanced anaerobic treatment of digested effluent from a 700 m3 chicken-manure continuous stirred tank reactor (CSTR). A 12.3 L internal circulation (IC) reactor inoculated with an anaerobic granular sludge and operated at 35 ± 1 °C was employed for the investigation. With a corresponding organic loading rate of 1.5-3.5 kg-COD/m3 d over a hydraulic retention time of 1.5 d, a maximum volumetric biogas production rate of 1.2 m3/m3 d and TCOD (total COD) removal efficiency ranging from 70% to 80% was achieved. However, the continual increase in the influent TAN content led to ammonia inhibition in the methanogenesis system. The SCOD/TAN (soluble COD/total ammonia nitrogen) ratio was presented to be the key controlling factor for the anaerobic treatment of semi-digested chicken manure, and further validation through shock loading and ammonia inhibition experiments was conducted. The threshold value of the SCOD/TAN ratio was determined to be 2.4 (corresponding to a TAN of 1250 mg/L) at an influent pH of 8.5-9. 相似文献
97.
Guangyong Zhu Xian Zhu Zuobing Xiao Rujun Zhou Yalun Zhu Xueliang Wan 《Journal of Material Cycles and Waste Management》2014,16(3):546-556
Biomass is recognized as an important solution to energy and the environmental problems related to fossil fuel usage. The rational utilization of biomass waste is important not only for the prevention of environmental issues, but also for the effective utilization of natural resources. Pyrolysis and hyrolysis in subcritical water are promising processes for biomass waste conversion. This paper deals with hydrolysis and pyrolysis of peanut shells. Hydrolysis and pyrolysis kinetics of peanut shell wastes were investigated for the in-depth exploration of process mechanisms and for the control of the reactions. Hydrolysis kinetics was conducted in a temperature range of 180–240 °C. A simplified kinetic model to describe the hydrolysis of peanut shells was proposed. Hydrolysis activation energy as well as the pre-exponential factor was determined according to the model. The target products of peanut shell hydrolysis, reducing sugars, can reach up to 40.5 % (maximum yield) at 220 °C and 180 s. Pyrolysis characteristics were investigated. The results showed that three stages appeared in this thermal degradation process. Kinetic parameters in terms of apparent pyrolysis activation energy and pre-exponential factor were obtained by the Coats–Redfern method. 相似文献
98.
99.
针对传统Fenton体系Fe(Ⅲ)累积和pH适用范围过窄等缺点,采用羟胺(HA)强化的HA-Fenton体系,以对氯苯酚(4-CP)为目标污染物进行降解实验,考察了Fe(Ⅱ)投加量、H2O2投加量、HA投加量和溶液pH等工艺条件对4-CP去除率的影响。实验结果表明:HA-Fenton体系适用于酸性和弱酸性条件,最佳pH范围为3.0~4.0;在溶液pH为3.0、Fe(Ⅱ)投加量为5.0 μmol/L、H2O2投加量为0.4 mmol/L、HA投加量为0.20 mmol/L的最适条件下,反应10 min, 4-CP去除率达64.25 %。 相似文献
100.
通过文献调研、问卷调查和典型样点采集的方法对吉林省3种主要覆膜作物的地膜残留情况进行调查分析,结果表明:地膜残留量与覆膜年限、地膜回收方式以及种植作物种类密切相关。随覆膜时间的延长地膜残留量有增加的趋势。3种模式地膜残留量由高到低为:瓜菜模式〉玉米连作模式〉花生连作模式,连续覆膜10年,3种模式的地膜残留量分别为30、28.35 kg·hm^-2和15.9kg·hm^-2。以一级污染水平作为标准(75 kg·hm^-2),覆膜量每年按75~150 kg·hm^-2、年残留率按1.2%~4.02%计,估算吉林省安全使用地膜的年限约为12~83年。 相似文献