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701.
702.
微污染水源水生物处理中硝酸盐氮的变化 总被引:2,自引:0,他引:2
通过中试系统和大型工程 ,探讨了微污染水源水生物处理工艺中硝酸盐氮的变化规律。研究表明 ,微污染水源水生物处理工艺中硝酸盐氮的增加是氨氮生物硝化的结果 ;处理系统启动中硝酸盐氮变化率的变化反映了两类硝化细菌在生长速率和转化能力上的协调关系以及生物膜的成熟过程 ,启动结束时硝酸盐氮变化率趋于 1.0 0 ;稳定运行阶段各工况下处理系统硝酸盐氮变化率均在 1.0 0附近 ;水源水中少量的有机氮和亚硝酸盐氮对氨氮硝化过程无明显影响。硝酸盐氮变化率是描述微污染水源水生物处理系统氨氮硝化状况的重要参数。 相似文献
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707.
郑州大气氮氧化物污染与灰色分析 总被引:2,自引:0,他引:2
通过对郑州市大气中NOx的监测和分析,初步揭示了NOx变化的规律。同时,运用灰色关联度分析,定量地分析了影响郑州市NOx变化的因素。并建立了该市的NOx产生量的GM(1,1)预测模型。结果表明:(1)影响NOx污染的主要因子是家庭用气普及率;(2)NOx在大气中的浓度呈逐年下降的趋势,2002年预测值为0.043mg/m^3。 相似文献
708.
An analytical solution for vertical transport of volatile chemicals in the vadose zone 总被引:1,自引:0,他引:1
An analytical solution is presented for one-dimensional vertical transport of volatile chemicals through the vadose zone to groundwater. The solution accounts for the important transport mechanisms of the steady advection of water and gas, diffusion and dispersion in water and gas, as well as adsorption, and first-order degradation. By assuming a linear, equilibrium partitioning between water, gas and the adsorbed chemical phases, the dependent variable in the mathematical model becomes the total resident concentration. The general solution was derived for cases having a constant initial total concentration over a discrete depth interval and a zero initial total concentration elsewhere. A zero concentration gradient is assumed at the groundwater table. Examples are given to demonstrate the application of the new solution for calculating the case of a non-uniform initial source concentration, and estimating the transport of chemicals to the groundwater and the atmosphere. The solution was also used to verify a numerical code called VLEACH. We discovered an error in VLEACH, and found that the new solution agreed very well with the numerical results by corrected VLEACH. A simplified solution to predict the migration of volatile organic chemical due to the gas density effect has shown that a high source concentration may lead to significant downward advective gas-phase transport in a soil with a high air-permeability. 相似文献
709.
In the present study, a hydrophilic bifunctional polymeric resin (LS-2) with sulfonic groups was synthesized, and the adsorption performance of three aniline compounds, aniline, 4-methylaniline, and 4-nitroaniline onto LS-2 was compared with that on the commercial Amberlite XAD-4. The uptake of the aniline compounds on LS-2 is a procedure of coexistence of physisorption and chemisorption and obeys the pseudo-second order rate equation, while the uptake of the compounds on XAD-4 is merely a physical adsorption and follows the pseudo-first order rate equation. All the isothermal data fit well with the Freundlich model, and the values of K(F) of the compounds adsorbing on LS-2 are much higher than those on XAD-4 suggesting the higher adsorbing capacities on LS-2 than those on XAD-4, which may be attributed to the microporous structure and the polar groups on the network of LS-2 resin. Dynamic adsorption and desorption studies for aniline on LS-2 show that the breakthrough adsorption capacity and the total adsorption capacity are 0.96 and 1.24 mmol per milliliter resin, respectively. Nearly 100% regeneration efficiency for the adsorbent was achieved by 5% hydrochloric acid. 相似文献
710.
Studies on applying the photochemical UV/TiO2 oxidation process to treat the lignin-containing wastewater for dissolved organic carbon (DOC), color and reducing A254 (the absorption at the wavelength of 254 nm) have been carried out. The data obtained in this study demonstrate that the UV/TiO2 process is effective in oxidizing the lignin thus reducing the color and DOC of the wastewater treated. The combined UV/TiO2 treatment can achieve better removal of DOC and color than the UV treatment alone. Color removal, based on American Dye Manufacture Index (ADMI) measurement, is greater than 99% if the pH is maintained at 3.0 with the addition of 1 g l(-1) TiO2. When 10 g l(-1) TiO2 is applied, the oxidation reduction potential (ORP) value is reached to result in an 88% removal of both DOC and color. A model was developed based on the variation of ORP during the photochemical reaction to simulate the decoloring process. The proposed model can be used to predict the color removal efficiency of the UV/TiO2 process. 相似文献