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991.
992.
Roy Mauldin Edward Kosciuch Fred Eisele Greg Huey David Tanner Steve Sjostedt Don Blake Gao Chen Jim Crawford Douglas Davis 《Atmospheric environment (Oxford, England : 1994)》2010,44(4):572-581
Measurements of OH, H2SO4, and MSA at South Pole (SP) Antarctica were recorded as a part of the 2003 Antarctic Chemistry Investigation (ANTCI 2003). The time period 22 November, 2003–2 January, 2004 provided a unique opportunity to observe atmospheric chemistry at SP under both natural conditions as well as those uniquely defined by a solar eclipse event. Results under natural solar conditions generally confirmed those reported previously in the year 2000. In both years the major chemical driver leading to large scale fluctuations in OH was shifts in the concentration levels of NO. Like in 2000, however, the 2003 observational data were systematically lower than model predictions. This can be interpreted as indicating that the model mechanism is still missing a significant HOx sink reaction(s); or, alternatively, that the OH calibration source may have problems. Still a final possibility could involve the integrity of the OH sampling scheme which involved a fixed building site. As expected, during the peak in the solar eclipse both NO and OH showed large decreases in their respective concentrations. Interestingly, the observational OH profile could only be approximated by the model mechanism upon adding an additional HOx radical source in the form of snow emissions of CH2O and/or H2O2. This would lead one to think that either CH2O and/or H2O2 snow emissions represent a significant HOx radical source under summertime conditions at SP. Observations of H2SO4 and MSA revealed both species to be present at very low concentrations (e.g., 5 × 105 and 1 × 105 molec cm?3, respectively), but similar to those reported in 2000. The first measurements of SO2 at SP demonstrated a close coupling with the oxidation product H2SO4. The observed low concentrations of MSA appear to be counter to the most recent thinking by glacio-chemists who have suggested that the plateau's lower atmosphere should have elevated levels of MSA. We speculate here that the absence of MSA may reflect efficient atmospheric removal mechanisms for this species involving either dynamical and/or chemical processes. 相似文献
993.
通过选用昆明市第五污水处理厂的一级A标出水和水处理厂外排污泥作为静态实验环境,研究不同混养密度下铜锈环棱螺、椭圆背角无齿蚌对污水处理厂再生水环境的净化性能,筛选出净化效果较好的放养密度。结果表明:放养30 d,铜锈环棱螺、椭圆背角无齿蚌对污水处理厂再生水环境的水质、底质均有一定的净化作用,扣减空白对照影响,水中COD、TP、NH3-N及底泥有机质平均去除率分别为22.26%、26.10%、25.60%和25.69%,底泥厚度平均减少3.8 cm;与对照相比,放养螺蚌45 d内水均能清澈见底,透明度均>70 cm,能明显稳定水体透明度,改善水环境。综合螺蚌生长适应性和净化效果考虑:污水处理厂再生水静态环境中,螺蚌混养密度应≤3 000 g/m3,在2 000~2 500 g/m3为宜,其中铜锈环棱螺的最适放养密度在400 g/m3,椭圆背角无齿蚌为1 600~2 100 g/m3。 相似文献
994.
995.
The octanol–air partition coefficients (KOA) for PBB15, PBB26, PBB31, PBB49, PBB103 and PBB153 were determined as a function of temperature using a gas chromatographic retention time technique with 1,1,1-trichloro-2,2-bis (4-chlorophenyl) ethane (p,p′-DDT) as a reference substance. The internal energies of phase change from octanol to air (ΔOAU) were calculated for the six compounds and were in the range from 74 to 116 kJ mol−1. Simple regression equations of log KOA versus relative retention times (RRTs) on gas chromatography (GC), and log KOA versus molecular connectivity indexes (MCI) were obtained, for which the correlation coefficients (r2) were greater than 0.985 at 283.15 K and 298.15 K. Thus the KOA values of the remaining PBBs can be predicted by using their RRTs and MCI according to these relationships. 相似文献
996.
Predicting the bioavailability of sediment-associated polybrominated diphenyl ethers using a 45-d sequential Tenax extraction 总被引:5,自引:0,他引:5
A 45-d Tenax extraction was used to evaluate the bioavailability of polybrominated diphenyl ethers (PBDEs) in three spiked sediments. The effect of aging on desorption kinetics of PBDEs was investigated by incubating one of the sediments for 7, 14, 30 and 60 d at room temperature. Desorption kinetics were well described by a three-compartment model. The fraction of very slow desorption (Fvs) contributed the most of the desorbed PBDEs from sediments. The total desorption amount of PBDEs decreased with the increase of total organic carbon in the sediments, suggesting that organic matter is an important factor controlling the partition of PBDEs in sediments. The total desorption amount of PBDEs decreased while log [(Fslow+Fvs)/Frap] increased with logKow of PBDE congeners, indicating that the bioavailability of PBDEs in sediment decreases with logKow of the congeners. As the residential time of PBDEs in the sediment increased from 7 to 60 d, Frap of individual PBDE congeners decreased gradually with simultaneous increase of Fvs. There was a good positive correlation between Frap and F6/F24, indicating that either 6 h or 24 h Tenax extraction could be a proxy for Frap and bioavailability. In general, the results in present study suggest that the bioavailability of nona- and deca-BDEs in sediment is very low due to their strong hydrophobicity and large molecular size. 相似文献
997.
曝气对潜流人工湿地中木本植物的影响 总被引:1,自引:0,他引:1
为了增加人工湿地植物的多样性,本文将花叶冬青(Ilex aquifolium)、月季(Rosa chinensis)和八角金盘(Fatsia japonica)3种木本植物引入潜流人工湿地,比较曝气前后系统对污水处理效果,植物的生物量与对TN、TP负荷减少的贡献率,根系形态与内部结构、根际微生物与基质酶活性的比较研究。结果表明,木本植物潜流人工湿地系统曝气后可以提高COD、NH4+-N、TN、TP的去除率,分别为6.99%、4.91%、10.25%、8.09%。湿地曝气有利于3种木本植物的生长,在曝气后比曝气前生物量增加了381.75、606.25和896.88 g/m2。曝气会促使木本植物长出大量须根,且曝气后的根系具有大量由薄壁细胞组成的通气组织的水生根特征。同时,曝气后增加了硝化菌数量,各处理单元中硝化菌增量分别为A:0.28 MPN×104/g,B:4.23 MPN×104/g,C:7.7 MPN×104/g。另外,曝气后植物根际基质中磷酸酶和尿酶的含量增加量大约在50%以上,这与系统中N和P的去除率提高的规律一致。 相似文献
998.
采用A/O-MBR系统,逐步提高进水氨氮浓度富集了硝化活性污泥(NAS),在此基础上,考察了COD、烯丙基硫脲(ATU)、氨氮初始浓度及氨氧化速率对NAS降解氧氟沙星(OFL)的影响。结果表明:富集的NAS的氨氧化速率达到了20 mg/(g SS·h)以上,对OFL具有明显降解作用;ATU存在条件下,COD对OFL的去除作用没有影响;提高初始氨氮浓度和NAS氨氧化速率均可以提高OFL降解量;初始氨氮浓度由50 mg/提升至150 mg/L时,OFL降解量由67.26 μg/g提高到82.11 μg/g;氨氧化速率由小于2.5 mg/(g SS·h)提升至大于20 mg/(g SS·h)时,OFL降解量由30.71 μg/g提高到75.16 μg/g。 相似文献
999.
Increasing polybrominated diphenyl ether (PBDE) contamination in sediment cores from the inner Clyde Estuary,UK 总被引:1,自引:0,他引:1
Christopher H. Vane Yun-Juan Ma She-Jun Chen Bi-Xian Mai 《Environmental geochemistry and health》2010,32(1):13-21
The concentrations of 16 polybrominated diphenyl ether (PBDE) congeners in six short sediment cores from the Clyde Estuary
were determined by gas-chromatography mass-spectrometry. Total PBDE concentrations ranged from 1 to 2,645 μg/kg and the average
concentration was 287 μg/kg. BDE-209 was the main congener and varied from 1 to 2,337 μg/kg. Elevated total PBDE concentrations
were observed close to the sediment surface in the uppermost 10 cm of four of the six sediment cores. Comparison of the down
core PBDE profiles revealed that the increase was driven by the accumulation of deca-BDE. Although the deca-BDE mix was dominant,
the presence of lower molecular weight congeners BDE-47, BDE-99, BDE-183 and BDE-153 at most sediment intervals suggested
additional sources of penta-BDE and octa-BDE pollution. Changing PBDE source input was the major factor in influencing the
proportion of nona-brominated congeners, although other explanations such as post burial photo-debromination of BDE-209 cannot
be entirely discounted. A clear cascading to lower hepta-, hexa-, and penta-homologues was not found. The increase in total
PBDE concentrations and particularly the deca-BDE may possibly be ascribed to the use and subsequent disposal of electrical
appliances such as televisions and computers. In the Clyde sediments, the proportion of nona-brominated congeners was higher
than that reported for commercial mixtures. This might be due to changing sources of PBDEs or post burial photo-debromination
of BDE-209. 相似文献
1000.