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211.
An area where a free-product accumulation of trichloroethylene (TCE) dense non-aqueous phase liquid (DNAPL) occurs at the bottom of a 10-m-thick surficial sand aquifer was studied to determine the integrity of the underlying, 20-m-thick, clayey silt aquitard formed of glaciolacustrine sediment. TCE concentration-versus-depth profiles determined from aquitard cores collected at five locations indicated penetration of detectable TCE 2.5 to 3.0 m into the aquitard. Two of the profiles show persistent DNAPL at the aquitard interface, while two others indicate that DNAPL, present initially, was completely dissolved away producing concentration declines at the aquitard interface. The fifth profile suggests shallow DNAPL penetration (<0.5 m) into the aquitard, however, this penetration, which was likely caused by cross-contamination during core collection or cone penetrometry (CPT) of the aquitard interface, did not increase the maximum depth of TCE penetration. Combining the field profiles with one-dimensional model simulations, downward migration of the aqueous TCE front, defined as the EPA MCL of 5 microg/l, which was below the analytical detection limit, was projected to a distance between 4 and 5 m below the top of the aquitard. Using a single set of estimated aquitard parameter values, simulations of aqueous TCE migration into the aquitard provided a good fit to four of the field profiles with a migration time of 35 to 45 years, consistent with the history of TCE use at the site. These simulations indicate aqueous TCE migration is diffusion-dominated with only small advective influence by the downward groundwater velocity of 2 to 3 cm/year or less in the aquitard due to pumping of the underlying aquifer to supply water to the facility in the past 50 years. The applicability of the parameter values was confirmed by in situ diffusion experiments of 1-year duration, in which stainless steel cylinders containing DNAPL were inserted into the aquitard. The diffusion-dominated nature of the profiles indicates that the aquitard provides long-term protection of the underlying aquifer from contamination from this DNAPL zone. Simulations of long-term migration of the TCE solute front indicate breakthrough to the lower aquifer at 1200 years for the no advection scenario and at 500 years if the strong downward hydraulic gradient persists. However, even after breakthrough, the mass flux through the aquitard to the underlying aquifer remains relatively low, and when considered in terms of potential impacts to pumping wells, concentrations are not expected to increase significantly above present-day MCLs. The use of contaminant profiles of different time and distance scales, in addition to hydraulic data, dramatically improves the ability to assess aquitard integrity, and provides improved transport parameter values for estimating contaminant arrival times and fluxes. The apparent lack of deep preferential pathways for TCE migration, such as open fractures, is probably due to the softness of the silty aquitard deposit and minimal physical or chemical weathering of the aquitard provides long-term protection of the underlying aquifer from contamination from this DNAPL zone. Simulations of long-term migration of the TCE solute front indicate breakthrough to the lower aquifer at 1200 years for the no advection scenario and at 500 years if the strong downward hydraulic gradient persists. However, even after the breakthrough, the mass flux through the aquitard to the underlying aquifer remains relatively low, and when considered in terms of potential impacts to pumping wells , concentrations are not expected to increase significantly above present-day MCLs. The use of contaminant profiles of different time and distance scales, in addition to hydraulic data, dramatically improves the ability to assess aquitard integrity, and provides improved transport parameter values for estimating contaminant arrival times and fluxes. The apparent lack of deep preferential pathways for TCE migration, such as open fractures, is probably due to the softness of the silty aquitard deposit and minimal physical or chemical weathering of the aquitard. 相似文献
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空气中挥发性有机物监测技术的研究进展 总被引:13,自引:0,他引:13
讨论了空气中挥发性有机化合物(VOCs)的监测分析方法研究进展。重点介绍了空气中VOCs的采集、分析和测定;简要叙述了样品前处理的新方法--固相微萃取法(SPME)与其它前处理方法的研究概况。 相似文献
215.
1 IntroductionInorganiccontaminants,phenolcompoundsaredeterminedprioritycontaminantbyUSEPA[1 ].ThephenolcompoundsinthedrinkingwaterisstipulatedasabsolutelydeterminationitembytheEuropeanEconomicCommunity (E E C .)andourcountry.Themeasurementofpollutionish… 相似文献
216.
Dynamics of Turbulence in Low-Speed Oscillating Bottom-Boundary Layers of Stratified Basins 总被引:1,自引:0,他引:1
Lorke Andreas Umlauf Lars Jonas Tobias Wüest Alfred 《Environmental Fluid Mechanics》2002,2(4):291-313
This paper focuses on the impact of an oscillating low-speed current on the structure and dynamics of the bottom-boundary layer (BBL) in a small stratified basin. A set of high-resolution current profile measurements in combination with temperature-microstructure measurements were collected during a complete cycle of the internal oscillation (`seiching') in the BBL of Lake Alpnach, Switzerland. It was found that even a relatively long seiching period of 24 hours significantly changed the form of the near-bottom current profiles as well as the dynamics of the turbulent dissipation rate compared to the steady-state law-of-the-wall. A logarithmic fit to the measured current profiles starting at a distance of 0.5 m above the sediment led to inconsistent estimates of both friction velocity and roughness length. Moreover, a phase lag between the current and the turbulent dissipation of 1.5 hours and a persistent maximum in the current profile at a height of 2.5 to 3 m above the sediment were observed. The experimental findings were compared to the results of a k- turbulence model and showed good agreement in general. Specifically, the inconsistent logarithmic fitting results and the observed phase lag were reproduced well by the model. 相似文献
217.
通过介绍环境空气中二氧化氮的测定方法──自动仪器监测法,对有关问题进行了初步探讨和研究,为正确使用该方法和仪器,确保监测工作的顺利进行提供了依据。 相似文献
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水相催化芳香氯化物脱氯研究 总被引:4,自引:0,他引:4
通过把起相转移作用的聚乙二醇(PEG)链,键合到硅胶上,再将聚乙烯吡咯烷酮(PVP)络合双金属Pd-Cu后负载其上,制成一种新型双负载双金属催化剂PVP-PdCl2/SiO2-PEG600,以甲酸钠为氢转移试剂,在水相催水芳香氯化物脱氯,当反应温度80℃左右,n(Pd):n(Cu)=2:1,反应介质pH值11.7左右时,具有较高的催化脱卤活性,催化剂不但易于制备,便于分离,且具有良好的重复使用性能,经重复使用六次,转化率仍在70%以上。 相似文献
220.