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1.
Catalytic activity of spinel ferrite in breaking down toxic dye materials are promising due to their uniqueness. In this study, aluminum-doped copper zinc ferrite, Cu0.4Zn0.6-xAlxFe2O4 (x = 0.0, 0.2, 0.4, 0.6), a catalyst for toxic dye degradation is synthesized through chemical co-precipitation route. The formation of the spinel ferrite catalyst is initially confirmed by Fourier transform infrared spectra, which shows the frequency of metal-oxygen bond vibration at 539 and 427 cm−1 attributed to the tetrahedral and octahedral sites respectively. Higher intensity sharp peak of X-ray diffraction for (311) plane is the evidence for the phase purity and the formation of spinel ferrite. The crystallite size is found to decrease with the increase of Al3+ ion. The surface structure of the obtained particles is investigated using a scanning electron microscope. Analyses of the material's magnetic characteristics using a vibrating sample magnetometer (VSM) revealed that it is, in fact, a soft magnet, as evidenced by the loop of its hysteresis, which is narrow. The catalytic degradation of methylene blue dye under the mechanism of the photo-Fenton process is studied with the obtained spinel ferrites and the result is found to be as high as 96.5%. The process follows pseudo-second order kinetics and the Langmuir isotherm.  相似文献   
2.
This study evaluated the hydrolysis and photolysis kinetics of pyraclostrobin in an aqueous solution using ultra-high-performance liquid chromatography–photodiode array detection and identified the resulting metabolites of pyraclostrobin by hydrolysis and photolysis in paddy water using high-resolution mass spectrometry coupled with liquid chromatography. The effect of solution pH, metal ions and surfactants on the hydrolysis of pyraclostrobin was explored. The hydrolysis half-lives of pyraclostrobin were 23.1–115.5?days and were stable in buffer solution at pH 5.0. The degradation rate of pyraclostrobin in an aqueous solution under sunlight was slower than that under UV photolysis reaction. The half-lives of pyraclostrobin in a buffer solution at pH 5.0, 7.0, 9.0 and in paddy water were less than 12?h under the two light irradiation types. The metabolites of the two processes were identified and compared to further understand the mechanisms underlying hydrolysis and photolysis of pyraclostrobin in natural water. The extracted ions obtained from paddy water were automatically annotated by Compound Discoverer software with manual confirmation of their fragments. Two metabolites were detected and identified in the pyraclostrobin hydrolysis, whereas three metabolites were detected and identified in the photolysis in paddy water.  相似文献   
3.
采用含有二乙二醇(DEG)和乙醇胺(ETA)的双组分解交联剂降解废旧硬质聚氨酯泡沫塑料(PU硬泡),并利用降解得到的低聚物多元醇与木质素复合制备出性能增强的再生PU硬泡。通过对制备的再生PU硬泡的红外光谱、密度、吸水率、抗压强度、热稳定性、导热系数、热重曲线等进行分析测试,考察m(DEG)∶m(ETA)对再生PU硬泡性能的影响。实验结果表明:m(DEG)∶m(ETA)=1∶3时废旧PU硬泡的降解效果最好;木质素加入量为2.0%(w)时再生PU硬泡的密度低、抗压强度高、保温性能良好,达到国家标准《建筑绝热用硬质聚氨酯泡沫塑料》(GB/T 21558—2008)的品质要求。  相似文献   
4.
The Yellow River is the second longest river in China and the cradle of the Chinese civilization. The source region of the Yellow River is the most important water holding area for the Yellow River, about 49.2% of the whole runoff comes from this region. However, for the special location, it is a region with most fragile eco-environment in China as well. Eco-environmental degradation in the source region of the Yellow River has been a very serious ecological and socially economic problem. According to census data, historical documents and climatic information, during the last half century, especially the last 30 years, great changes have taken place in the eco-environment of this region. Such changes are mainly manifested in the temporal-spatial changes of water environment, deglaciation, permafrost reduction, vegetation degeneracy and desertification extent, which led to land capacity decreasing and river disconnecting. At present, desertification of the region is showing an accelerating tendency. This paper analyzes the present status of eco-environment degradation in this region supported by GIS and RS, as well as field investigation and indoor analysis, based on knowledge, multi-source data is gathered and the classification is worked out, deals with their natural and anthropogenic causes, and points out that in the last half century the desertification and environmental degradation of this region are mainly attributed to human activities under the background of regional climate changes. To halt further degradation of the environment of this region, great efforts should be made to use land resources rationally, develop advantages animal agriculture and protect the natural grassland.  相似文献   
5.
The structure and function of the coastal wetland ecosystem in the southern Laizhou Bay have been changed greatly and influenced by regional hydrological changes. The coastal wetlands have degraded significantly during the latest 30 years due to successive drought, decreasing of runoff, pollution, underground saline water intrusion, and aggravating marine disasters such as storm tides and sea level rising. Most archaic lakes have vanished, while artificial wetlands have been extending since natural coastal wetlands replaced by salt areas and ponds of shrimps and crabs. The pollution of sediments in inter-tidal wetlands and the pollution of water quality in sub-tidal wetlands are getting worse and therefore “red tides” happen more often than before. The biodiversity in the study area has been decreased. Further studies are still needed to protect the degraded coastal wetlands in the area.  相似文献   
6.
不同来源土样胶体对氯霉素吸附行为的影响   总被引:1,自引:0,他引:1  
选取不同来源沉积物或土壤样品(沉积物A1和A2,天然土壤B1和B2,市售营养土B3),采用切向超滤与多种纳米分析技术相结合的方法,分析了不同土样中胶体的理化特征及其对氯霉素(CAP)吸附行为的影响.荧光区域积分法结果显示,土样胶体的荧光组分以色氨酸类蛋白质、类富里酸和类腐殖酸为主,络氨酸类蛋白质和溶解性微生物代谢物质存在较少.吸附实验结果表明,B3胶体对CAP的吸附率最大(36.25%),在胶体浓缩液和超滤液中的分配比例最高(1.91),但其有机碳归一化结合系数最低(3.93).与天然土壤相比,河湖沉积物胶体的吸附率较高,但其与CAP的结合能力却较低.冗余分析结果表明,胶体对CAP的吸附主要与其芳香度、有色溶解性有机质丰度、溶解性有机碳浓度及分子量有关;此外,胶体的腐殖化程度、芳环上羧基、羰基等官能团的比重及荧光物质中溶解性微生物代谢产物和类腐殖酸对CAP的吸附行为也具有较大影响.  相似文献   
7.
以二溴硝基甲烷为研究,采用单一控制变量法研究了光照强度、初始物浓度、自由氯、溴离子、pH值等影响因子对二溴硝基甲烷光降解的影响,探讨了二溴硝基甲烷的光降解动力学规律.结果表明:二溴硝基甲烷在紫外光条件下的降解遵循一级反应动力学规律,其光降解效率随二溴硝基甲烷初始浓度的增加而减小,随光照强度和pH值增加而增加;溴离子的存在能促进二溴硝基甲烷的光降解;添加自由氯能够显著加快二溴硝基甲烷的光降解效率,并且会使二溴硝基甲烷在光降解的过程中转化为以一溴一氯硝基甲烷为主的其他卤代硝基甲烷.此研究结果可为水处理过程中控制二溴硝基甲烷的形成、降低水质安全风险提供参考.  相似文献   
8.
周茹  朱君 《中国环境科学》2020,40(4):1429-1436
利用2013年地基CE-318太阳光度计观测数据,结合中分辨率成像光谱仪(MODIS)遥感产品和HYSPLIT后向轨迹分析,研究了一次东南亚生物质燃烧污染长距离输送至中国西南昆明站点过程(2013年4月5~8日)中,气溶胶光学特性和辐射特性的变化及其可能来源.结果表明,此次污染过程期间,我国西南地区生物质燃烧活动较少,而中南半岛地区生物质燃烧活动显著.4月5~7日,昆明站点气溶胶光学厚度(AOD)升高,消光波长指数(EAE)和吸收波长指数(AAE)均增大.此外,依据EAE和AAE分类方法,5~6日昆明站点以城市工业气溶胶为主,7~8日以生物质燃烧气溶胶为主,其细模态峰值半径(0.11μm)小于5~6日(0.15μm),7日细模态粒子体积浓度峰值(约为0.16μm3/μm2)是5日的2倍.气溶胶直接辐射强迫(ARF)日变化结果表明4月7日气溶胶对地表的降温效应达到最大,对大气的加热作用最强.气溶胶直接辐射强迫效率值(ARFE)的变化表明生物质燃烧气溶胶对大气顶的降温作用减弱.MODIS遥感以及HYSPLIT模式后向轨迹表明,此次昆明站点生物质燃烧气溶胶主要来源于东南亚地区(主要是印度北部、印缅北部和不丹地区).  相似文献   
9.
To clarify the aerosol hygroscopic growth and optical properties of the Pearl River Delta(PRD)region,integrated observations were conducted in Heshan City of Guangdong Province from October 19 to November 17,2014.The concentrations and chemical compositions of PM_(2.5),aerosol optical properties and meteorological parameters were measured.The mean value of PM_(2.5) increased from less than 35(excellent) to 35-75 μg/m~3(good) and then to greater than 75 μg/m~3(pollution),corresponding to mean PM_(2.5) values of 24.9,51.2,and 93.3 μg/m~3,respectively.The aerosol scattering hygroscopic growth factor(f(RH = 80%)) values were 2.0,2.12,and 2.18 for the excellent,good,and pollution levels,respectively.The atmospheric extinction coefficient(σext)and the absorption coefficient of aerosols(σ_(ap)) increased,and the single scattering albedo(SSA)decreased from the excellent to the pollution levels.For different air mass sources,under excellent and good levels,the land air mass from northern Heshan had lower f(RH) and σ_(sp) values.In addition,the mixed aerosol from the sea and coastal cities had lower f(RH) and showed that the local sources of coastal cities have higher scattering characteristics in pollution periods.  相似文献   
10.
Understanding the degradation behavior of azo dyes in photocatalytic wastewater treatment is of fundamental and practical importance for their application in textile-processing and other coloration industries. In this study, quantum chemistry, as density functional theory, was used to elucidate different degradation pathways of azo pyridone dyes in a hydroxyl radical (HO?)-initiated photocatalytic system. A series of substituted azo pyridone dyes were synthesized by changing the substituent group in the para position of the benzene moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The effect of dye molecular structure on the photocatalytic degradation reaction mechanism was analyzed and quantification of substituent effects on the thermodynamic and kinetics parameters was performed. Potential energy surface analysis revealed the most susceptible reaction site for the HO? attack. The calculated reaction barriers are found to be strongly affected by the nature of substituent group with a good correlation using Hammett σp constants and experimentally determined reaction rates. The stability of pre-reaction complexes and transition state complexes were analyzed applying the distortion-interaction model. The increased stability of the transition state complexes with the distancing from the substituent group has been established.  相似文献   
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