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991.
992.
以粉煤厌为原料采用两步法合成了2种单一沸石矿物种的NaA和NaX型沸石,并对产物的结构和性能进行了详细表征.2种沸石产物的吸附性能比较结果表明,NaA型沸石优于NaX型沸石.在静态吸附条件下,研究了NaA型沸石吸附水溶液中Cr(Ⅵ)的相关参数(溶液pH值、吸附温度和吸附时间),并用Langmuir和Freundlich等温吸附线对吸附结果进行拟和.结果表明:Cr(Ⅵ)的吸附行为符合Langmuir方程;饱和吸附量为47.78 mg/g.NaA型沸石对Cr(Ⅵ)的吸附是物理和化学吸附两种行为共同作用的结果. 相似文献
993.
994.
Guo R Li X Christie P Chen Q Zhang F 《Environmental pollution (Barking, Essex : 1987)》2008,151(3):443-451
Two-year greenhouse cucumber experiments were conducted to investigate seasonal effects on fruit yield, dry matter allocation, and N uptake in a double-cropping system with different fertilizer management. Seasonal effects were much greater than fertilizer effects, and winter-spring (WS) cucumber attained higher fruit yields and N uptake than autumn-winter (AW) cucumber due to lower cumulative air temperatures during fruit maturation in the AW season. Fertilizer N application and apparent N loss under recommended N management (Nmr) decreased by 40-78% and 33-48% without yield loss compared to conventional N management (Nmt) over four growing seasons. However, there were no seasonal differences in N recommendations, taking into consideration seasonal differences in crop N demand, critical nutrient supply in the root zone and N mineralization rate. 相似文献
995.
淀山湖沉水植物死亡分解过程中营养物质的释放 总被引:8,自引:0,他引:8
测定了上海淀山湖5种常见沉水植物的营养成分含量及其死亡后在好氧(DO>3.5 mg/L)或低氧(DO<3.5 mg/L)状态下分解释放TN、TP和有机物(以高锰酸盐指数计,下同)等营养物质的动态过程,并对营养物质释放强度与营养成分含量的相关性进行了分析.结果表明, 5种沉水植物中,金鱼藻的TN和TP含量最高,质量分数分别为(4.07±0.22)%和(0.99±0.09)%;好氧状态下TN和有机物的释放强度大于低氧状态,两种状态下TP的释放强度没有显著差异;TP的释放比TN快,一般需10 d左右,而TN和有机物的释放分别需要29 d和20 d左右;在好氧状态下,NO-2-N、NO-3-N和可溶性总磷酸盐的平均释放强度与植物TN含量呈显著正相关(p<0.05),NH 4-N的平均释放强度与植物TP含量呈显著正相关(p<0.05);在低氧状态下,NO-2-N的平均释放强度与植物TN含量、NO-3-N的平均释放强度与植物TP含量分别呈显著正相关(p<0.05);有机物的平均释放强度与植物TP含量呈极显著负相关(p<0.01). 相似文献
996.
基于SWAT模型的流域面源污染模拟影响分析 总被引:4,自引:0,他引:4
针对流域面源污染模型往往忽略或简化河道内污染物变化过程的缺陷,探讨了河道水质模型对流域面源污染模拟的影响.以太湖流域浙西区的西苕溪流域为研究对象,选取具有一定物理机制的分布式面源污染模型SWAT模型,分别以激活和不激活其嵌套的河道水质模型QUAL2E,即SWAT模型与QUAL2E模型紧密耦合和松散耦合两种情况进行模拟,并比较了对TN及TP的模拟效果.结果表明,丰水期与平水期的模拟结果并没有显著差别;但在枯水期,由于水量较小,河道内污染物变化过程对模拟结果影响较大.同时引入QUAL2K模型,分析认为改进河道水质模型对提高SWAT模型模拟精度有一定的效果. 相似文献
997.
伞罩型除尘脱硫塔内除雾器性能研究 总被引:1,自引:0,他引:1
除雾器是湿法烟气脱硫(WFGD)系统内重要的设备之一,其性能对WFGD系统运行的可靠性有重要影响.利用Fluent6.2软件对新型伞罩型除尘脱硫塔内的三维两相流场进行数值模拟,气相采用RNG湍流模型,液相采用离散相模型,选择SIMPLE算法进行计算,分析塔内的折板除雾器和旋流板除雾器的速度场、压力场和液滴的分布情况.结果表明,烟气经过折板除雾器,产生了明显的压降,且在拐角区域湍流耗散强烈,是实现气液分离的关键区域;烟气经过旋流板除雾器,速度和压强分布具有良好的对称性,液滴被气流旋转抛向壁面实现气液分离.模拟结果对新型的WFGD除雾器的设计和运行具有一定的理论指导意义. 相似文献
998.
Environmental contaminants with estrogenic activity have recently attracted attention due to their potential detrimental effects on the reproduction of human and wildlife. The aim of this study was to evaluate the use of endogenous glutathione and glutathione-related enzymes as biomarkers of exposure to landfill leachate effluent and bisphenol A (BPA) in the freshwater snail, Bellamya purificata. Following exposure to 1%, 5% and 10% landfill leachate effluent and 1, 10, 50 and 100mugl(-1) BPA for 0, 2, 7 and 15d, activities of glutathione S-transferase (GST), selenium-dependent glutathione peroxidase (SeGPx) and glutathione reductase (GR) and levels of total glutathione were measured in the gills and digestive glands of the snails. GST and total glutathione were the most sensitive parameters in both exposure scenarios. GST activities increased by about 80%, while total glutathione decreased to 70% and 80% in the gills and digestive glands, respectively. In contrast, SeGPx and GR activities remained at the same levels in all the treatment groups compared with those of controls. The results indicated that among glutathione and glutathione-related enzymes, GST activity and total glutathione level, which showed dose-dependent dynamics, could be used as biomarkers of aquatic ecosystems contaminated with landfill leachate. 相似文献
999.
A strategy for aromatic hydrocarbon bioremediation under anaerobic conditions and the impacts of ethanol: a microcosm study 总被引:7,自引:0,他引:7
Increased use of ethanol-blended gasoline (gasohol) and its potential release into the subsurface have spurred interest in studying the biodegradation of and interactions between ethanol and gasoline components such as benzene, toluene, ethylbenzene and xylene isomers (BTEX) in groundwater plumes. The preferred substrate status and the high biological oxygen demand (BOD) posed by ethanol and its biodegradation products suggests that anaerobic electron acceptors (EAs) will be required to support in situ bioremediation of BTEX. To develop a strategy for aromatic hydrocarbon bioremediation and to understand the impacts of ethanol on BTEX biodegradation under strictly anaerobic conditions, a microcosm experiment was conducted using pristine aquifer sand and groundwater obtained from Canadian Forces Base Borden, Canada. The initial electron accepter pool included nitrate, sulfate and/or ferric iron. The microcosms typically contained 400 g of sediment, 600 approximately 800 ml of groundwater, and with differing EAs added, and were run under anaerobic conditions. Ethanol was added to some at concentrations of 500 and 5000 mg/L. Trends for biodegradation of aromatic hydrocarbons for the Borden aquifer material were first developed in the absence of ethanol, The results showed that indigenous microorganisms could degrade all aromatic hydrocarbons (BTEX and trimethylbenzene isomers-TMB) under nitrate- and ferric iron-combined conditions, but not under sulfate-reducing conditions. Toluene, ethylbenzene and m/p-xylene were biodegraded under denitrifying conditions. However, the persistence of benzene indicated that enhancing denitrification alone was insufficient. Both benzene and o-xylene biodegraded significantly under iron-reducing conditions, but only after denitrification had removed other aromatics. For the trimethylbenzene isomers, 1,3,5-TMB biodegradation was found under denitrifying and then iron-reducing conditions. Biodegradation of 1,2,3-TMB or 1,2,4-TMB was slower under iron-reducing conditions. This study suggests that addition of excess ferric iron combined with limited nitrate has promise for in situ bioremediation of BTEX and TMB in the Borden aquifer and possibly for other sites contaminated by hydrocarbons. This study is the first to report 1,2,3-TMB biodegradation under strictly anaerobic condition. With the addition of 500 mg/L ethanol but without EA addition, ethanol and its main intermediate, acetate, were quickly biodegraded within 41 d with methane as a major product. Ethanol initially present at 5000 mg/L without EA addition declined slowly with the persistence of unidentified volatile fatty acids, likely propionate and butyrate, but less methane. In contrast, all ethanol disappeared with repeated additions of either nitrate or ferric iron, but acetate and unidentified intermediates persisted under iron-enhanced conditions. With the addition of 500 mg/L ethanol and nitrate, only minor toluene biodegradation was observed under denitrifying conditions and only after ethanol and acetate were utilized. The higher ethanol concentration (5000 mg/L) essentially shut down BTEX biodegradation likely due to high EA demand provided by ethanol and its intermediates. The negative findings for anaerobic BTEX biodegradation in the presence of ethanol and/or its biodegradation products are in contrast to recent research reported by Da Silva et al. [Da Silva, M.L.B., Ruiz-Aguilar, G.M.L., Alvarez, P.J.J., 2005. Enhanced anaerobic biodegradation of BTEX-ethanol mixtures in aquifer columns amended with sulfate, chelated ferric iron or nitrate. Biodegradation. 16, 105-114]. Our results suggest that the apparent conservation of high residual labile carbon as biodegradation products such as acetate makes natural attenuation of aromatics less effective, and makes subsequent addition of EAs to promote in situ BTEX biodegradation problematic. 相似文献
1000.
Distribution characteristics of nonylphenolic chemicals in Masan Bay environments, Korea 总被引:3,自引:0,他引:3
To understand the distribution characteristics of nonylphenolics and sterols, samples such as in creek water, sea surface water, waste water treatment plant (WWTP) effluent water, sediment and mussel were collected and analyzed. The principal analytes are nonylphenol (NP), nonylphenol monoethoxylate (NP1EO), nonylphenol diethoxylate (NP2EO), coprostanol (5beta) and cholestanol (5alpha). All these target pollutants showed 100% detection frequency in all of the samples analyzed. Total concentration of nonylphenolic compounds ranged from 334 to 3628ngl(-1) (average: 1331ngl(-1)) in creek water, from 15 to 36400ngl(-1) (average: 1013ngl(-1)) in sea surface water, from 131 to 2811ngg(-1) dry weight (average: 581ngg(-1) dry weight) in sediment and from 50.5 to 289ngg(-1) dry weight (average: 139ngg(-1) dry weight) in mussel. For water samples, levels of nonylphenolics determined in summer season were higher than those in spring season. Among them, nonylphenol and NP1EO was dominant in creek water and seawater, respectively. The highest concentration was recorded in sediment near a WWTP effluent outlet. And high levels of nonylphenolics and sterols were found in about 3km area surrounding WWTP effluent outlet. Coefficient of linear regression (R(2)) for NP in mussel and in sediment was 0.90. Similarly good correlation (R(2)=0.98) was obtained between concentration in water and in mussel indicating that a steady state has been reached in this bay. The calculated bio concentration factor (BCF=2990) for NP in Masan Bay agrees well with reported values in the literature. 相似文献