首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   4734篇
  免费   190篇
  国内免费   1753篇
安全科学   315篇
废物处理   292篇
环保管理   351篇
综合类   2438篇
基础理论   782篇
污染及防治   1930篇
评价与监测   174篇
社会与环境   187篇
灾害及防治   208篇
  2024年   3篇
  2023年   81篇
  2022年   233篇
  2021年   174篇
  2020年   122篇
  2019年   124篇
  2018年   188篇
  2017年   216篇
  2016年   269篇
  2015年   303篇
  2014年   375篇
  2013年   495篇
  2012年   378篇
  2011年   435篇
  2010年   313篇
  2009年   288篇
  2008年   305篇
  2007年   250篇
  2006年   266篇
  2005年   188篇
  2004年   148篇
  2003年   155篇
  2002年   159篇
  2001年   148篇
  2000年   156篇
  1999年   146篇
  1998年   154篇
  1997年   114篇
  1996年   106篇
  1995年   81篇
  1994年   67篇
  1993年   58篇
  1992年   54篇
  1991年   27篇
  1990年   36篇
  1989年   12篇
  1988年   9篇
  1987年   12篇
  1986年   7篇
  1985年   4篇
  1984年   2篇
  1983年   5篇
  1982年   3篇
  1981年   3篇
  1979年   2篇
  1978年   2篇
  1977年   1篇
排序方式: 共有6677条查询结果,搜索用时 11 毫秒
91.
Liao CH  Kang SF  Wu FA 《Chemosphere》2001,44(5):1193-1200
Simultaneous effect of inorganic anions, such as chloride and bicarbonate ions, on the scavenging of hydroxyl radicals (HO*) in the H2O2/UV process is the focus of this paper. The model compound of n-chlorobutane (BuCl) was used as the probe of HO*. By changing the pH conditions (2-9) and the concentrations of NaCl (0.25-2500 mM) and NaHCO3 (25 mM), the variation of HO* concentrations and the rate of H2O2 decomposition were compared. In general, the BuCl and H2O2 follow closely the first-order reaction within the first 10 and 40 min, respectively. In the presence of chloride alone at the pH range of 2-6, the HO* concentration in the reaction mixture increases with the increase of pH, and the HO* concentration at pH = 6 is 100 times of that at pH = 2. Including bicarbonate species in the solution, the peak HO* concentration was found at a certain pH, which shifts from 4, 5, to 5-7, as the molar ratios of chloride/bicarbonate species increase from 1 to 100. In addition, without bicarbonate species HO* concentration decreases significantly with increasing chloride concentration but remained rather unchanged beyond 1250 mM. In contrast, the HO* scavenging in the presence of bicarbonate species became relatively significant only when the chloride concentration reached beyond 250 mM. Throughout all experiments of different water quality conditions, the H2O2 decomposition rate remains rather unchanged.  相似文献   
92.
This paper reports the influences of the herbicide butachlor (n-butoxymethlchloro -2', 6'-diethylacetnilide) on microbial populations, respiration, nitrogen fixation and nitrification, and on the activities of dehydrogenase and hydrogen peroxidase in paddy soil. The results showed that the number of actinomycetes declined significantly after the application of butachlor at different concentrations ranging from 5.5 microg g(-1) to 22.0 microg g(-1) dried soil, while that of bacteria and fungi increased. Fungi were easily affected by butachlor compared to the bacteria. The growth of fungi was retarded by butachlor at higher concentrations. Butachlor however, stimulated the growth of anaerobic hydrolytic fermentative bacteria, sulfate-reducing bacteria (SRB) and denitrifying bacteria. The increased concentration of butachlor applied resulted in the higher number of SRB. Butachlor inhibited the growth of hydrogen-producing acetogenic bacteria. The effect of butachlor varied on methane-producing bacteria (MPB) at different concentrations. Butachlor at the concentration of 1.0 microg g(-1) dried soil or less than this concentration accelerated the growth of MPB, while at 22.0 microg g(-1) dried soil showed an inhibition. Butachlor enhanced the activity of dehydrogenase at increasing concentrations. The soil dehydrogenase showed the highest activity on the 16th day after application of 22.0 microg g(-1) dried soil of butachlor. The hydrogen peroxidase could be stimulated by butachlor. The soil respiration was depressed during the period from several days to more than 20 days, depending on concentrations of butachlor applied. Both the nitrogen fixation and nitrification were stimulated in the beginning but reduced greatly afterwards in paddy soil.  相似文献   
93.
Wu Z  Zhou M  Wang D 《Chemosphere》2002,48(10):1089-1096
A novel electrocatalysis method for phenol degradation was described using a β-PbO2 anode modified with fluorine resin and a Ni–Cr–Ti alloy cathode. In case of air sparging at the cathodic zone, the techniques of anodic–cathodic electrocatalysis (ACEC) and ferrous ion catalyzed anodic–cathodic electrocatalysis (FACEC) in the presence of iron(II) were developed. Both of ACEC and FACEC were more effective than anodic electrocatalysis (AEC). The percentage of phenol eliminated by FACEC could increase by nearly 30% compared with that of AEC, and the current efficiency could reach to 70%. Important operating factors such as ferrous ion concentration, air-sparging rate and applied current were investigated and it was found that such beneficial effects could be achieved at a suitable current and ratio of the concentration of ferrous ion to the air sparged. The mechanism of phenol degradation is proposed to be the generation of hydroxyl radicals concerned with the two electrodes. Results also indicated that the process provided an efficient way to regenerate ferrous ion compared with the conventional Fenton's system.  相似文献   
94.
Aquatic hypoxia caused by eutrophication may lead to mass mortality of valuable living resources such as fish and shrimp. However, there is little information on the hypoxic tolerance of penaeid shrimp, and whether they are able to avoid hypoxia. In laboratory experiments, LC50, LT50 and heart beats per minute were determined for juvenile Metapenaeus ensis at 0.5, 1.0, 2.0 and 6.0 mg O2 l(-1). The 8-h LC50, for DO was 0.77 mg O2 l(-1), while the LT50 at 0.5 mg O2 l(-1) was 399 min. Heart beat rate significantly declined when DO fell below 1.0 mg O2 l(-1). When confronted with a gradient of dissolved oxygen, M. ensis were able to avoid hypoxic areas and move to oxygenated water. M. ensis appeared to be sensitive to hypoxia, and their ability to detect and avoid hypoxia may enhance their survival in habitats where hypoxia may occur.  相似文献   
95.
As a primary factor responsible for lake eutrophication, a deeper understanding of the phosphorus (P) composition and its turnover in sediment is urgently needed. In this study, P species in surface sediments from a Chinese large eutrophic lake (Lake Taihu) were characterized by traditional fractionation and 31P nuclear magnetic resonance (NMR) spectroscopy, and their contributions to the overlying water were also discussed. Fractionation results show that NaOH-P predominated in the algal-dominated zone, accounting for 60.1% to total P in Zhushan Bay. Whereas, refractory fractions including HCl-P and residual-P were the main P burial phases in the macrophyte-dominated zone, the center and lakeshore. Recovery rates of the total P and organic P were greatly improved by using a modified single-step extraction of NaOH-EDTA, ranging from 22.6 to 66.1% and from 15.0 to 54.0%. Ortho-P, monoester-P, and pyro-P are identified as the major P components in the NaOH-EDTA extracts by 31P NMR analysis. Trace amount of DNA-P appeared only in sediments from algal- and macrophyte-dominated zones, ascribing to its biological origin. The relative content of ortho-P is the highest in the algal-dominated zone, while the biogenic P including ester-P and pyro-P is the highest in the macrophyte-dominated zone. Moreover, ortho-P and pyro-P correlated positively with TP and chlorophyll a in the overlying water, whereas only significant relationships were found between monoester-P, biogenic P, and chlorophyll a. These discrepancies imply that inorganic P, mainly ortho-P, plays a vital role in sustaining the trophic level of water body and algal bloom, while biogenic P makes a minor contribution to phytoplankton growth. This conclusion was supported by the results of high proportion of biogenic P in algae, aquatic macrophytes, and suspended particulate from the published literature. This study has significant implication for better understanding of the biogeochemical cycling of endogenous P and its role in affecting lake eutrophication.  相似文献   
96.
中低温厌氧处理城市污水污泥颗粒化的研究   总被引:2,自引:0,他引:2  
用高径比为3:1的UASB反应器分别在35℃和室温条件下处理模拟城市污水,研究了污泥的颗粒化过程.比较了在不同温度、浓度下形成的颗粒污泥的特征.水温为9~25℃,进水浓度为100~200 mg COD/L,水力上流速度(Vup)在0.013~0.11 m/h的4^#UASB反应器在60 d内在形成了成熟的颗粒污泥.研究表明,进水中低的有机物浓度,低的Ca^2+、Mg^2+浓度和低的Vup没有抑制颗粒化进程.  相似文献   
97.
推导了BAF前置反硝化工艺简化动力学模型,揭示了BAF去除有机物与反应速率常数与膜厚的关系。同时以生物膜中活性物质与非活性物质增长生物数学模型体系为基础,从理论上推导了BAF最佳膜厚的范围。  相似文献   
98.
Cd(Ⅱ)-邻菲咯啉络合物极谱吸附波测定水中微量镉   总被引:3,自引:0,他引:3  
在PH=4.74的0.2mol/HAc-NaAc缓冲体系中,Cd(Ⅱ)-邻菲咯啉络合物在单扫描波极谱仪上于-0.79V处产生一灵敏的吸附还原波,其二次微分极谱波灵敏度高,波形好。  相似文献   
99.
W H Ding  J Wu  M Semadeni  M Reinhard 《Chemosphere》1999,39(11):1781-1794
The occurrence and behavior of wastewater indicator compounds in the Santa Ana River (SAR) water and the underlying aquifer recharged by the SAR has been studied. The SAR contains a high proportion of tertiary treated wastewater effluents, up to 100% during summer and fall. The following water quality parameters were quantified: four specific wastewater indicator compounds, ethylene diaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), a naphthalene dicarboxylate (NDC) isomer, alkylphenol polyethoxy carboxylates (APECs), and selected haloacetic acids (HAAs), nitrate, dissolved oxygen (DO), DOC, total carbohydrate, and phenolic substances. Statistical analysis indicated that normal distribution was adequate to describe the probability distribution of the constituents in most cases. In the river, the concentrations of wastewater indicator compounds decreased as the fraction of storm runoff increased. EDTA and NDC were detected in a monitoring well near the river and in two production wells 1.8 and 2.7 km down gradient with little apparent attenuation. By contrast, NTA, APECs, bromochloro- and dibromoacetic acids appeared to be attenuated significantly during infiltration of river water and groundwater transport.  相似文献   
100.
Data from long-term groundwater sampling, limited coring, and associated studies are synthesised to assess the variability and intrinsic remediation/natural attenuation of a dissolved hydrocarbon plume in sulphate-rich anaerobic groundwater. Fine vertical scale (0.25- and 0.5-m depth intervals) and horizontal plume-scale (>400 m) characteristics of the plume were mapped over a 5-year period from 1991 to 1996. The plume of dissolved BTEX (benzene, toluene, ethylbenzene, xylene) and other organic compounds originated from leakage of gasoline from a subsurface fuel storage tank. The plume was up to 420 m long, less than 50 m wide and 3 m thick. In the first few years of monitoring, BTEX concentrations near the point of leakage were in approximate equilibrium with non-aqueous phase liquid (NAPL) gasoline. NAPL composition of core material and long-term trends in ratios of BTEX concentrations in groundwater indicated significant depletion (water washing, volatilisation and possibly biodegradation) of benzene from residual NAPL after 1992. Large fluctuations in BTEX concentrations in individual boreholes were shown to be largely attributable to seasonal groundwater flow variations. A combination of temporal and spatial groundwater quality data was required to adequately assess the stationarity of plumes, so as to allow inference of intrinsic remediation. Contoured concentration data for the period 1991 to 1996 indicated that plumes of toluene and o-xylene were, at best, only partially steady state (pseudo-steady state) due to seasonal groundwater flow changes. From this analysis, it was inferred that significant remediation by natural biodegradation was occurring for BTEX component plumes such as toluene and o-xylene, but provided no conclusive evidence of benzene biodegradation. Issues associated with field quantification of intrinsic remediation from groundwater sampling are highlighted. Preferential intrinsic biodegradation of selected organic compounds within the BTEX plume was shown to be occurring, in parallel with sulphate reduction and bicarbonate production. Ratios of average hydrocarbon concentrations to benzene for the period 1991 to 1992 were used to estimate degradation rates (half-lives) at various distances along the plume. The estimates varied with distance, the narrowest range being, for toluene, 110 to 260 days. These estimates were comparable to rates determined previously from an in situ tracer test and from plume-scale modelling.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号