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721.
通过恒温振荡平衡法研究了Pb~(2+)在针铁矿上的等温吸附和吸附动力学特征,探讨了吸附的影响因素.结果表明:(1)随Pb~(2+)平衡浓度和pH的增大,针铁矿对Pb~(2+)的吸附量逐渐增大.(2)针铁矿对Pb~(2+)的等温吸附可用Freundlich和Langmuir方程较好地拟合.(3)在相同温度和pH下,随离子强度的提高,针铁矿对Pb~(2+)的吸附量增大.(4)在相同离子强度和pH下,针铁矿对Pb~(2+)的吸附量总体随温度升高而增大.针铁矿对Pb~(2+)的吸附是自发进行的吸热反应.(5)针铁矿吸附Pb~(2+)的过程可分为初始的快吸附和随后的慢吸附2个阶段.pH影响吸附反应快慢,随pH增大吸附速率增大;随着pH的增大,达到平衡吸附的时间缩短.吸附动力学方程用Elovich方程拟合最佳.  相似文献   
722.
以传统卫生填埋柱R2为对照,通过往生物反应器填埋柱R1内加载可渗透反应介质层1和2进行模拟试验,主要探讨了填埋柱R1垃圾渗滤液COD、总氮、氨氮及总磷的变化趋势,探索一种新型的加载介质层垃圾填埋处理方法。试验结果表明,填埋20周后, R1柱COD浓度基本维持在40 000~45 000 mg/L间,约为R2柱的20%~30%;第24周,R1柱总氮和氨氮分别为206.5 mg/L和167.3 mg/L,在16~24周内,R1总氮和氨氮分别约为R2的14.5%~17.5%和36.2%~43.6%;18周时,R1柱总磷达最大值1.704 mg/L,至第24周降为0.673 mg/L, 整个实验过程R1柱总磷约为R2的0.15%~0.56%。  相似文献   
723.
光合细菌强化二级流化床工艺处理焦化废水的研究   总被引:1,自引:0,他引:1  
采用厌氧酸化加二级流化床组合工艺处理焦化废水。一级反应器内光合细菌与兼性厌氧菌处于共生状态,二级反应器内光合细菌与亚硝酸细菌处于共生状态。一级反应器内光合细菌有充分的小分子有机酸可降解并形成二次酸化,在二级反应器内完成进一步降解。结合反应条件:温度,pH,DO和基质浓度等,将二级反应器内硝化反应控制在亚硝化阶段,有效地保证了废水中碳源的利用。稳定运行了60 d,结果显示,出水COD和NH3-N浓度分别为105~135 mg/L和14~20 mg/L,去除率分别稳定在90.3%~92.5%和92%~95%。TN去除率稳定在83%~86%。酚、氰化物和BOD5的去除率均在95%以上。  相似文献   
724.
硝酸盐对反硝化除磷过程的影响分析   总被引:4,自引:1,他引:3  
在厌氧/缺氧间歇反应器内考察了硝酸盐进水浓度及进水方式对反硝化除磷过程的影响。结果表明:在缺氧阶段,反硝化除磷菌(DPBs)可将硝酸盐转化为亚硝酸盐,当硝酸盐浓度较低时,DPBs以亚硝酸盐为电子受体吸磷。进水COD浓度为220 mg/L,正磷浓度为6.8 mg/L,硝酸盐初始浓度为26 mg/L时,系统达到最佳脱氮除磷效果,期间亚硝酸盐浓度积累至10.71 mg/L。采用连续流投加硝酸盐的方式更利于氮磷的高效去除。  相似文献   
725.
高锰酸钾降解地下水中PCE的研究   总被引:2,自引:1,他引:1  
田璐  杨琦  尚海涛 《环境工程学报》2009,3(8):1355-1359
以氯代有机污染物中常见的PCE为目标污染物,以自制高锰酸钾溶液为氧化剂,采用批实验方法,探讨了高锰酸钾降解PCE的反应动力学、影响因素以及反应机理。反应结果表明,高锰酸钾降解PCE的反应符合一级动力学方程,反应活化能E为57.119 kJ/mol,在30℃条件下,反应速率常数为0.0076 min-1,半衰期为91.20 min。在pH在3~10,离子强度在0~0.1030 mol/L之间变化时,反应速率不受明显影响。  相似文献   
726.
超细粉煤灰基成型吸附剂的动态吸附实验   总被引:2,自引:1,他引:1  
以粉煤灰为原料制备成型吸附剂,对水溶液中亚甲基蓝和Cr6+进行动态吸附研究,绘制穿透曲线,利用Origin软件对实验数据分析处理,得出穿透曲线的通式Ct=A1A2〖〗1+(t/t0)p+A1。结果表明,初始浓度C0=25 mg/L,填料高度不同时,达到穿透点的时间随填料高度的增加而增加;填料高度h=200 mm,初始浓度不同时,达到穿透点的时间随初始浓度的增加而减小;该吸附剂对有机染料和重金属离子均有较好的吸附性能;穿透曲线通式的回归线性相关系数表明,该通式可很好地反映超细粉煤灰成型吸附剂的动态吸附过程。  相似文献   
727.
厌氧序批式反应器内挥发性脂肪酸积累特性研究   总被引:1,自引:0,他引:1  
小试规模的厌氧序批式反应器(ASBR),通过人工配水,研究了启动3个月时间以及一个运行周期内反应器内挥发性脂肪酸(VFA)的积累情况,并通过分析期间产甲烷活性的变化说明了控制VFA积累的重要性。经过近120 d的运行,乙酸和丙酸的最大比产甲烷活性分别提高了1.8和2.2倍,说明反应器的启动过程即是微生物群落的优化和选择的过程,ASBR的抗冲击的能力较强说明随启动的进行和种群的优化,活性污泥凝聚性能增强,对VFA的降解能力增强。  相似文献   
728.
Modeling potential herbicide loss to surface waters on the Swiss plateau   总被引:1,自引:0,他引:1  
Lack of sufficiently detailed data often limits the applicability of complex transport-reaction models for estimating potential herbicide loss to surface waters. Therefore, there is also a need for simple models that are easy to apply but still capture the main features of the underlying processes.In this study, a simple regression model was developed to assess the vulnerability of catchments in the Swiss Plateau to diffuse herbicide loss to surface waters. The model is designed as a screening tool to rank the catchments in a relative sense and not to calculate Predicted Environmental Concentrations (PEC) of pesticides. The main goal is to capture two dominating factors controlling diffuse herbicide transport into streams and rivers. These factors are herbicide application and fast flow processes that are mainly responsible for herbicide transport. In a first step vulnerability of sites to herbicide loss is estimated based on site-specific conditions irrespective of actual herbicide application. In the second step, this vulnerability assessment is combined with actual herbicide application data to estimate the potential herbicide loss.The fast flow index (FFI), derived from discharge data using a base flow separation method, was applied as a proxy for the amount of fast flow occurring. The influence of catchment attributes (including topographic, climatic and soil data) on the FFI was analyzed using a multiple regression approach based on data from 57 catchments of the Swiss Plateau. By combining regression analysis with mechanistic knowledge, a two factor non-linear model based on river density and soil permeability as dominant input factors was selected as the best model for FFI prediction given the available data. Higher dimensional models had to be excluded because the strong correlation between the potential input factors led to unrealistic dependences while only minimally improving the quality of the fit.The spatial pattern of the predicted FFI as a measure for the vulnerability to diffuse herbicide losses shows a clearly increasing trend from the western to the eastern part of the Swiss Plateau and towards the pre-alpine/alpine regions in the south.In general the pattern of herbicide use corresponds to site conditions typical of a low FFI. However, the spatial analysis revealed exceptions, namely areas in which high actual herbicide use coincides with a high FFI.Despite the uncertainties in the model, this simple approach seems to be useful for supporting site-adapted agricultural practice whenever the higher accuracy of more detailed models is not required or too expensive to achieve. In addition, in combination with data on actual herbicide application, it can support the design of monitoring strategies by identifying critical areas of actual herbicide loss.  相似文献   
729.
Lignocellulosic materials are good precursors for the production of activated carbon. In this work, coffee residue has been used as raw material in the preparation of powder activated carbon by the method of chemical activation with zinc chloride for the sorption of Pb(II) from dilute aqueous solutions.The influence of impregnation ratio (ZnCl2/coffee residue) on the physical and chemical properties of the prepared carbons was studied in order to optimize this parameter. The optimum experimental condition for preparing predominantly microporous activated carbons with high pore surface area (890 m2/g) and micropore volume (0.772 cm3/g) is an impregnation ratio of 100%. The developed activated carbon shows substantial capability to sorb lead(II) ions from aqueous solutions and for relative impregnation ratios of 75 and 100%, the maximum uptake is practically the same. Thus, 75% represents the optimal impregnation ratio.Batch experiments were conducted to study the effects of the main parameters such as contact time, initial concentration of Pb(II), solution pH, ionic strength and temperature. The maximum uptake of lead(II) at 25 °C was about 63 mg/g of adsorbent at pH 5.8, initial Pb(II) concentration of 10 mg/L, agitation speed of 200 rpm and ionic strength of 0.005 M. The kinetic data were fitted to the models of pseudo-first order and pseudo-second order, and follow closely the pseudo-second order model. Equilibrium sorption isotherms of Pb(II) were analyzed by the Langmuir, Freundlich and Temkin isotherm models. The Freundlich model gives a better fit than the others.Results from this study suggest that activated carbon produced from coffee residue is an effective adsorbent for the removal of lead from aqueous solutions and that ZnCl2 is a suitable activating agent for the preparation of high-porosity carbons.  相似文献   
730.
In the present study, an adsorbent was prepared from tamarind seeds and used after activation for the removal of Cr(VI) from aqueous solutions. The tamarind seeds were activated by treating them with concentrated sulfuric acid (98% w/w) at a temperature of 150 °C. The adsorption of Cr(VI) was found to be maximum at low values of initial pH in the range of 1–3. The adsorption process of Cr(VI) was tested with Langmuir, Freundlich, Redlich–Peterson, Koble–Corrigan, Tempkin, Dubinin–Radushkevich and Generalized isotherm models. Application of the Langmuir isotherm to the system yielded a maximum adsorption capacity of 29.7 mg/g at an equilibrium pH value ranging from 1.12 to 1.46. The adsorption process followed second-order kinetics and the corresponding rate constants obtained were 2.605 × 10−3, 0.818 × 10−3, 0.557 × 10−3 and 0.811 × 10−3 g/mg min−1 for 50, 200, 300 and 400 mg/L of initial Cr(VI) concentration, respectively. The regenerated activated tamarind seeds showed more than 95% Cr(VI) removal of that obtained using the fresh activated tamarind seeds. A feasible solution is proposed for the disposal of the contaminants (acid and base solutions) containing high concentrations of Cr(VI) obtained during the regeneration (desorption) process.  相似文献   
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