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301.
研究了泥水体系中柠檬酸-Fe(Ⅱ)/K2SO8降解敌草隆时各影响因子的作用机制,通过正交实验确定了反应的最佳操作条件为:K2SO8浓度为2.0mmol/L,Fe(Ⅱ)浓度为1.0mmol/L,柠檬酸浓度为0.5mmol/L,反应时间为120min,pH=7.0。此奈件下,0.1mmol/L敌草隆降解率可达97.6%。采用分子探针竞争实验鉴定了体系中产生的硫酸根自由基。 相似文献
302.
303.
以国际腐殖质协会(IHSS)推荐的胡敏酸提取方法为基础,以去有机质土壤中添加胡敏酸所配制的土壤为研究对象,引入超声作为胡敏酸提取的辅助条件,采用批次试验优化了土壤中胡敏酸的提取方法。结果表明,基于胡敏酸提取回收率和精密度,在室温下获得的优化提取方法为:液土比为8:1、提取次数为3次、Na OH溶液浓度为0.05 mol/L、超声功率为120 W、超声时间为30 min;在此优化条件下,胡敏酸的回收率为94.73%±1.50%,显著大于IHSS推荐方法的回收率64.76%±0.28%,变异系数CV为1.59%、小于10%。相对于IHSS提取法,此优化提取法具有胡敏酸提取回收率高、资源节约、胡敏酸变性小、提取时间短等优点。 相似文献
304.
Photo-catalytic decolourisation of toxic dye with N-doped titania: A case study with Acid Blue 25 总被引:1,自引:0,他引:1
Dyes are one of the hazardous water pollutants.Toxic Acid Blue 25,an anthraquinonic dye,has been decolourised by photo-catalysing it with nitrogen doped titania in aqueous medium.The photo catalyst was prepared from 15% TiCl 3 and 25% aqueous NH 3 solution as precursor.XRD and TEM revealed the formation of well crystalline anatase phase having particle size in the nano-range.BET surface area of the sample was higher than that of pure anatase TiO 2.DRS showed higher absorption of radiation in visible range compared to pure anatase TiO 2.XPS revealed the presence of nitrogen in N-Ti-O environment.The experimental parameters,namely,photocatalyst dose,initial dye concentration as well as solution pH influence the decolourisation process.At pH 3.0,the N-TiO 2 could decolourise almost 100% Acid Blue 25 within one hour.The influence of N-TiO 2 dose,initial concentration of Acid Blue 25 and solution pH on adsorption-desorption equilibrium is also studied.The adsorption process follows Lagergren first order kinetics while the modified Langmuir-Hinselwood model is suitably fitted for photocatalytic decolourisation of Acid Blue 25. 相似文献
305.
Qianni Zhou Chunlei Cheng Suxia Yang Minghao Yuan Jingjing Meng Haifeng Gong Qien Zhong Yao Zhang Yutong Xie Zhen Zhou Mei Li 《环境科学学报(英文版)》2022,34(1):185-196
Black carbon(BC) plays an important role in air quality and climate change, which is closely associated with its mixing state and chemical compositions. In this work the mixing state of BC-containing single particles was investigated to explore the evolution process of ambient BC particles using a single particle aerosol mass spectrometer(SPAMS) in March 2018 in Zhengzhou, China. The BC-containing particles accounted for 61.4% of total detected ambient single particles and were classified into f... 相似文献
306.
应用开顶式熏气装置,以油菜、白菜、波菜、青茭和蕃茄为材料,分别暴露于模拟酸性降水(pH2.8~5.6)单一污染和模拟酸性降水与SO2复合污染的环境,测定其生理代谢、生长和产量的反应。结果指出:酸性降水和SO2复合处理对叶绿素含量,光合强度,叶片K+外渗,叶片含糖量和相对生长速率的影响大于单独酸性降水和SO2处理,五种蔬菜在酸性降水(pH5.6~2.8)和SO2(0.1ppm)复合处理下,减产6.0%~29.0%,表现为协同效应,比酸性降水和SO2单独处理的危害更大。 相似文献
307.
珠江三角洲酸雨及其造成的农作物损失的研究 总被引:6,自引:0,他引:6
探讨了珠江三角洲酸雨高发的原因,并估算了珠江三角洲因酸雨和SO2污染而造成的农作物的经济损失。 相似文献
308.
1987-1989年春秋季在西南重庆、贵阳、成都和广元等地区采集大气颗粒物和雨水样品,测定了其中S和SO4^2-。探讨了颗粒物中S在粗细粒中的分布及水溶性S的百分比,估算了大气中S在气相(SO2)、液相(H2SO4)及固相(SO4^2-)中的分配比例,得知颗粒物中S对降雨的贡献率为18~50%。 相似文献
309.
The chemical composition of throughfall and canopy leaching, as well as the acid neutralizing capacity and alkalinity depended on the age of Norway spruce (Picea abies Karst) stands and season of the year. A higher amount of sulphur and strong acids was deposited to the soil in the older age classes. Concentrations of SO(4)(2)(-), K(+), H(+), Mn(2+), Fe(2+) and Zn(2+) in throughfall were higher than in bulk precipitation in any season. This suggests that these ions were washed out or washed from the surface of needles and/or barks. The other ions NO(3)(-), NH(4)(+), Ca(2+) and Mg(2+) were retained by the canopy, in particular Ca(2+) and Mg(2+) during the growing season in young stands. Principal component analysis identified five factors responsible for the data structure and suggested the major anthropogenic emission sources were acidic emission (SO(4)(2)(-)+NO(3)(-)), heavy metals-dust particles (Fe(2+)+Mn(2+)+Zn(2+)), ammonium (NH(4)(+)) and H(+), while the natural-origin emission was mineral dust (Na(+)+K(+)+Ca(2+)+Mg(2+)). 相似文献
310.
Chapman PJ Clark JM Reynolds B Adamson JK 《Environmental pollution (Barking, Essex : 1987)》2008,151(1):110-120
Much uncertainty still exists regarding the relative importance of organic acids in relation to acid deposition in controlling the acidity of soil and surface waters. This paper contributes to this debate by presenting analysis of seasonal variations in atmospheric deposition, soil solution and stream water chemistry for two UK headwater catchments with contrasting soils. Acid neutralising capacity (ANC), dissolved organic carbon (DOC) concentrations and the Na:Cl ratio of soil and stream waters displayed strong seasonal patterns with little seasonal variation observed in soil water pH. These patterns, plus the strong relationships between ANC, Cl and DOC, suggest that cation exchange and seasonal changes in the production of DOC and seasalt deposition are driving a shift in the proportion of acidity attributable to strong acid anions, from atmospheric deposition, during winter to predominantly organic acids in summer. 相似文献