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211.
Nanoscale zero-valent iron(n ZVI) particles supported on a porous, semi-interpenetrating(semi-IPN), temperature-sensitive composite hydrogel(PNIPAm-PHEMA). n ZVI@PNIPAmPHEMA, was successfully synthesized and characterized by FT-IR, SEM, EDS, XRD and the weighing method. The loading of nZVI was 0.1548 ± 0.0015 g/g and the particle size was30–100 nm. NZVI was uniformly dispersed on the pore walls inside the PNIPAm-PHEMA.Because of the well-dispersed n ZVI, the highly porous structure, and the synergistic effect of PNIPAm-PHEMA, nZVI@PNIPAm-PHEMA showed excellent reductive activity and wide p H applicability. 95% of 4-NP in 100 m L of 400 mg/L 4-NP solution with initial p H 3.0–9.0 could be completely reduced into 4-AP by about 0.0548 g of fresh supported n ZVI at 18–25 °C under stirring(110 r/min) within 45 min reaction time. A greater than 99% 4-NP degradation ratio was obtained when the initial p H was 5.0–9.0. The reduction of 4-NP by nZVI@PNIPAm-PHEMA was in agreement with the pseudo-first-order kinetics model with Kobsvalues of 0.0885–0.101 min-1.NZVI@PNIPAm-PHEMA was able to be recycled, and about 85% degradation ratio of 4-NP was obtained after its sixth reuse cycle. According to the temperature sensitivity of PNIPAmPHEMA, n ZVI@PNIPAm-PHEMA exhibited very good storage stability, and about 88.9%degradation ratio of 4-NP was obtained after its storage for 30 days. The hybrid reducer was highly efficient for the reduction of 2-NP, 3-NP, 2-chloro-4-nitrophenol and 2-chloro-4-nitrophenol. Our results suggest that PNIPAm-PHEMA could be a good potential carrier, with n ZVI@PNIPAm-PHEMA having potential value in the application of reductive degradation of nitrophenol pollutants.  相似文献   
212.
Herein,with the exploitation of iron and nickel electrodes,the 2,4-dichlorophenol(2,4-DCP)dechlorinating processes at the anode and cathode,respectively,were separately studied via various electrochemical techniques(e.g.,Tafel polarization,linear polarization,electrochemical impedance spectroscopy).With this in mind,Ni/Fe nanoparticles were prepared by chemical solution deposition,and utilized to test the dechlorination activities of 2,4-DCP over a bimetallic system.For the iron anode,the results showed that higher 2,4-DCP concentration and solution acidity aggravated the corrosion within the electrode.The charge transfer resistance(R_(ct))values of the iron electrode were 703,473,444,and 437Ω·cm~2 for the initial 2,4-DCP concentrations of0,20,50,and 80 mg/L,respectively.When the bulk pH of the 2,4-DCP solution varied from 3.0,5.0to 7.0,the corresponding R_(ct) values were 315,376,and 444Ω·cm~2,respectively.For the nickel cathode,the reduction current densities on the electrode at-0.75 V(vs.saturated calomel electrode)were 80,106,and 111μA/cm~2,for initial 2,4-DCP concentrations of 40,80,and125 mg/L.The dechlorination experiments demonstrated that when the initial pH of the solution was 7.0,5.0,and 3.0,the dechlorination percentage of 2,4-DCP by Ni/Fe nanoparticles was 62%,69%,and 74%,respectively,which was in line with the electrochemical experiments.10 wt.%Ni loading into Ni/Fe bimetal was affordable and gave a good dechlorination efficiency of 2,4-DCP,and fortunately the Ni/Fe nanoparticles remained comparatively stable in the dechlorination processes at pH 3.0.  相似文献   
213.
在纤维干燥尾气的余热回收利用中,飞灰沉积会直接影响设备的安全高效运行,不利于木材工业的节能减排。阐述了飞灰沉积机理和数值模拟等研究现状。对于弹性球形颗粒的沉积,已获得了一些科学可靠的机理模型和论证结果,为灰污防治提供了合理的技术支持;关于柔性细长颗粒的沉积,仅取得少量的成果,需要进一步全面深入展开相关研究。  相似文献   
214.
Deposition of aerosols in the respiratory system depends inter alia on their size and the respiratory tract deposition is appreciable for nanometer-sized particles. This article presents the results of measurements of size distributions of aerosols in the range of several nanometers up to about 20?μm in the underground mine excavations of an active hard coal mine. The study included practically all particles of a respirable fraction. The results showed that a high concentration of fine and ultrafine aerosols occurs in key underground workplaces especially during mining machine operations, although their contribution to total mass concentration is usually negligible.  相似文献   
215.
In the present study, air pollutant concentrations have been analyzed statistically with meteorological factors in the city of Elazig, which is located in the east Anatolia region of Turkey, for the months of September, October, November, December, January, February, March, and April during the years 2003 and 2004. SPSS code was used for statistical analyses. The relationship between monitored air pollutant concentrations, such as SO2 and the total suspended particles (TSP) data, and meteorological factors such as wind speed, temperature, relative humidity and pressure was investigated. According to the results of linear and non-linear regression analysis, it was found that there is a moderate and weak level of relation between the air pollutant concentrations and the meteorological factors in Elazig. The correlation between the previous day's SO2, TSP concentrations and actual concentrations of these pollutants on that day was investigated and the coefficient of determination R was found to be 0.80 and 0.76, respectively. The statistical models of SO2 and TSP, including all of the meteorological parameters, gave an R of 0.50 and 0.40, respectively. Further, in order to develop this model, the previous day's SO2 and TSP concentrations were added to the equations. The new model for SO2 and TSP was improved considerably with R = 0.85 and 0.80, respectively.  相似文献   
216.
Danish rivers carry >50% of the phosphorus (P) transport as particulate P (PP). In five of six rivers sampled in November 1998 iron-bound P made up > 59% of PP and loosely adsorbed P ranged between 2% and 13%. This fraction could potentially be released in 14‰ seawater. The behaviour of dissolved and particulate P fractions was studied during seven month in a 2 km long estuary with low freshwater retention time and low tidal range. The river carried ∼10% of PP as loosely adsorbed P but increased concentrations of dissolved inorganic P (DIP) relative to the estuarine mixing line was only observed in the summer month with low freshwater flow and was more likely due to DIP release from the bottom sediment. Instead estuarine particles were always enriched with oxidized iron (ox.Fe) and iron-bound P as well as loosely adsorbed P and during May–September this coincided with increasing concentration of PP in estuary. We suggest that flocculation of ox.Fe and adsorption of DIP onto the particles with subsequent transport seawards is a major loss process for P during the summer month. During winter month where 85% of the run-off occurs the dominant process in the estuary is sedimentation of larger particles, however, a comparison of river particles with surface sediment clearly reveals that most PP is mobilized again from the bottom sediments.  相似文献   
217.
三维粒子电极催化氧化活性艳红X-3B实验研究   总被引:2,自引:1,他引:1  
采用浸渍焙烧法制备了Cu/γ-Al2O3、Cu-Co/γ-Al2O3粒子电极,TiO2/Ti为阳极、石墨为阴极,采用三维电极降解染料模拟废水活性艳红X-3B溶液,考察了粒子电极、槽电压、pH值、电解质浓度等因素对处理效果的影响。实验结果表明:该反应器能够有效的降解X-3B,粒子电极显示了较高的催化活性,双组分粒子电极Cu-Co/γ-Al2O3比单组分粒子电极Cu/γ-Al2O3有着更好的催化效果,降解机制主要是电致·OH的间接氧化和粒子电极表面的直接氧化的协同作用。  相似文献   
218.
大气细颗粒物水溶成分和非水溶成分的细胞毒性   总被引:7,自引:1,他引:6  
为了研究细颗粒物不同成分细胞毒作用的差异,以细颗粒物水溶成分和非水溶成分对人肺癌上皮细胞株A549细胞染毒.结果表明,在染毒剂量为100 μg·mL-1、200 μg·mL-1和300 μg·mL-1的范围内,水溶成分的细胞毒性明显高于非水溶成分(P(0.05),表现为抑制细胞活性,导致细胞膜损伤增加.并且诱导细胞活性氧(ROS)的产生.使用N-乙酰半胱氨酸(NAC)和抗坏血酸(Vit C)阻断活性氧(ROS)产生的研究结果表明,与未加上述抗氧化剂的染毒组相比,加抗氧化剂的染毒组细胞的活性明显增强.因此,提示细颗粒物水溶成分是最主要的毒性成分之一,而氧化.应激损伤可能是细颗粒物细胞毒作用的重要机制之一.  相似文献   
219.
Nanoscale palladized iron(Pd/Fe)bimetallic particles were prepared by reductive deposition method.The particles were characterized by X-ray diffraction(XRD),X-ray fluorescence(XRF),scanning electron microscope(SEM),transmission electron microscope(TEM),and Brunauer-Emmett-Teller-nitrogen(BET-N_2)method.Data obtained from those methods indicated that nanoscale Pd/Fe bimetallic particles containedα-Fe~0.Detected Pd to Fe ratio by weight(Pd/Fe ratio)was close to theoretical value. Spherical granules with di...  相似文献   
220.
上流式曝气生物滤池两种填料启动挂膜的试验研究   总被引:3,自引:2,他引:1  
在相同运行条件下,对瓷粒和陶粒2种不同填料曝气生物滤池(BAF)的启动运行进行了实验研究,考察了不同填料在挂膜过程中CODCr和NH4^+-N的去除效果及出水NO2^--N和NO3^--N质量浓度的变化。结果表明,在常温下(20~25℃)2种填料的所需的启动时间差异较大,陶粒填料所需时间为17d,而瓷粒填料别需37d。启动挂膜过程中,两者对CODCr和NH4^+-N可达到基本相同的去除率,但所需运行时间差异较大,陶粒BAF较之瓷粒BAF稳定,且硝化效果好于瓷粒BAF.  相似文献   
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