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481.
研究以纳米TiO2为载体,浸渍负载过渡金属氧化物,以CO为还原剂的脱硝催化剂的脱硝性能。实验中以计算量的Ni(NO3)2和Fe(NO3)3混合溶液浸渍纳米TiO2粉末,室温下搅拌30 min至混合均匀,放入旋转蒸发器中,70℃下至水分蒸干为止;所得粉末在550℃下、空气气氛中焙烧4 h即得所需催化剂。用以上方法分别制备2%Fe2O3-10%Cr2O3/TiO2、4%Fe2O3-8%Cr2O3/TiO2、6%Fe2O3-6%Cr2O3/TiO2、8%Fe2O3-4%Cr2O3/TiO2与10%Fe2O3-2%Cr2O3/TiO2等5种催化剂样品。实验结果表明,制备的催化剂具有较好的结构,分散较为均匀。对于CO+NO反应,Fe2O3-Cr2O3/TiO2系列催化剂具有较好的催化活性,NO的转化率都达到了100%。其中,10%Fe2O3-2%Cr2O3/TiO2样品具有最好的低温活性,H2-TPR结果表明,这是由于10%Fe2O3-2%Cr2O3/TiO2催化剂更易于被CO预还原。 相似文献
482.
This study investigated the aerobic degradation of tetrabromobisphenol-A (TBBPA) and changes in the microbial community in river sediment from southern Taiwan. Aerobic degradation rate constants (k1) and half-lives (t1/2) for TBBPA (50 μg g−1) ranged from 0.053 to 0.077 d−1 and 9.0 to 13.1 d, respectively. The degradation of TBBPA (50 μg g−1) was enhanced by adding yeast extract (5 mg L−1), sodium chloride (10 ppt), cellulose (0.96 mg L−1), humic acid (0.5 g L−1), brij 30 (55 μM), brij 35 (91 μM), rhamnolipid (130 mg L−1), or surfactin (43 mg L−1), with rhamnolipid yielding a higher TBBPA degradation than the other additives. For different toxic chemicals in the sediment, the results showed the high-to-low order of degradation rates were bisphenol-A (BPA) (50 μg g−1) > nonylphenol (NP) (50 μg g−1) > 4,4′-dibrominated diphenyl ether (BDE-15) (50 μg g−1) > TBBPA (50 μg g−1) > 2,2′,3,3′,4,4′,5,5′,6,6′-decabromodiphenyl ether (BDE-209) (50 μg g−1). The addition of various treatments changed the microbial community in river sediments. The results also showed that Bacillus pumilus and Rhodococcus ruber were the dominant bacteria in the process of TBBPA degradation in the river sediments. 相似文献
483.
The behaviors and fate of polycyclic aromatic hydrocarbons (PAHs) in a coking wastewater treatment plant 总被引:4,自引:0,他引:4
The occurrence, behaviors and fate of 18 PAHs were investigated in a coking wastewater treatment plant in Songshan coking plant, located in Shaoguan, Guangdong Province of China. It was found that the target compounds occurred widely in raw coking wastewater, treated effluent, sludge and gas samples. In raw coking wastewater, high molecular weight (MW) PAHs were the dominant compounds, while 3-6 ring PAHs predominated in the final effluent. The dominant compounds in gas samples were phenathrene, fluoranthene and pyrene, while they were fluoranthene, pyrene, chrysene and benzo[k]fluoranthene for sludge. The process achieved over 97% removal for all the PAHs, 47-92% of eliminations of these target compounds in liquid phase were achieved in biological stage. Different behaviors of PAHs were observed in the primary tank, anaerobic tank, aerobic tank, hydrolytic tank and coagulation tank units, while heavier and lower ones were mainly removed in anaerobic tank and aerobic tanks, respectively. Regarding the fate of PAHs, calculated fractions of mass losses for low MW PAHs due to transformation and adsorption to sludge accounted for 15-50% and 24-49%, respectively, while the rest was less than 1%. For high MW PAHs, the mass losses were mainly due to adsorption to sludge and separation with tar (contributing 56-76% and 22-39%, respectively), and the removal through transformation was less. 相似文献
484.
Ren M Peng P Cai Y Chen D Zhou L Chen P Hu J 《Environmental pollution (Barking, Essex : 1987)》2011,159(5):1375-1380
The study presented the concentrations and distributions of polybrominated dibenzo-p-dioxins and polybrominated dibenzofurans (PBDD/Fs) as impurities in some commercial decabromodiphenyl ether (DBDE) mixtures that were produced by several manufacturers. The total concentrations of 12 2,3,7,8-substituted tetra- to octa-BDD/F congeners were found to be in the range of 3.4-13.6 (mean 7.8) μg/g, averagely accounting for 99% of total PBDD/Fs. OBDF was the prevailing congener, followed by 1,2,3,4,6,7,8-HpBDF. In addition, OBDD and 1,2,3,4,7,8-HxBDF were also obviously detectable. The total concentrations of PBDD/Fs varied both between the manufacturers and between the lots. On the basis of the global demand for the commercial DBDE in 2001, the annual potential emissions of PBDD/Fs were calculated coarsely to be 0.43 (range: 0.21-0.78) tons. The major dioxin congeners, OBDF and 1,2,3,4,6,7,8-HpBDF, presenting in DBDE, were estimated to be formed from BDE-209, BDE-206, and/or BDE-207 via an intra-molecular elimination of Br2/HBr. 相似文献
485.
Gao P Feng Y Zhang Z Liu J Ren N 《Environmental pollution (Barking, Essex : 1987)》2011,159(10):2876-2881
Knowledge of toxic chemical sorption by soil/sediment is critical for environmental risk assessment of toxic chemicals, especially for the multi-sorbate system in river ecosystem. Sorption characteristics of 2, 4-Dichlorophenol, 2, 4-Dinitrophenol and 2, 4-Dimethyphenol on sediment were investigated. Adsorption isotherms in single- and multi-sorbate systems fitted well the Freundlich model. The adsorption effects were different among three selected phenolic compounds in single- and multi-sorbate systems. The synergetic affect that 2, 4-Dinitrophenol and 2, 4-Dimethyphenol bring to 2, 4-Dichlorophenol can be explained by the compression of double electronic layer and the charge neutrality. Adsorption kinetic results showed that pseudo-second-order model can be used to describe the experimental data and the adsorption affinity of phenolic compounds influenced greatly by the adsorption velocity. The present study suggests that the fate and transport of emerging pollutants such as phenolic compounds could be affected in the presence of different hydrophobic pollutants in aquatic systems. 相似文献
486.
Wang H Ouyang Z Chen W Wang X Zheng H Ren Y 《Environmental pollution (Barking, Essex : 1987)》2011,159(8-9):2127-2137
Transpiration rates of six urban tree species in Beijing evaluated by thermal dissipation method for one year were correlated to environmental variables in heat, water, and pollutant groups. To sort out colinearity of the explanatory variables, their individual and joint contributions to variance of tree transpiration were determined by the variation and hierarchical partitioning methods. Majority of the variance in transpiration rates was associated with joint effects of variables in heat and water groups and variance due to individual effects of explanatory group were in comparison small. Atmospheric pollutants exerted only minor effects on tree transpiration. Daily transpiration rate was most affected by air temperature, soil temperature, total radiation, vapor pressure deficit, and ozone. Relative humidity would replace soil temperature when factors influencing hourly transpiration rate was considered. 相似文献
487.
利用ICP-AES分析了潞城市采暖期和非采暖期4个不同功能区PM10样品中16种化学元素,对不同元素的时空分布特征进行了研究,并采用富集因子和主成分分析初步研究了潞城市PM10中元素的主要来源。结果表明,潞城市PM10中重金属污染较为严重,且各元素在采暖期的平均浓度均明显高于非采暖期。PM10中Ca、V、Cr、As、Ni、Mn、Cu、Zn、Al和Pb的富集因子EF〉10,主要来源于人为污染;而Na、Mg、Si、Fe和K的EF〈10,除部分来自人为活动外,主要来自土壤风沙等自然来源。主成分分析结果显示,潞城市PM10中元素的主要来源按贡献率大小依次为:煤烟尘和工业粉尘50.39%,自然源34.37%和机动车尾气15.24%。 相似文献
488.
489.
490.
用于地表水反硝化的纤维素碳源选择研究 总被引:1,自引:0,他引:1
为了选取合适的天然有机物作为反硝化细菌碳源用于解决地表水中NO3--N污染问题,以江南大学校内湖水为接种物,选取8种天然纤维素碳源在缺氧状态不同的处理方式下对60 mg/L NO3--N的降解特性进行研究。结果表明,以碱处理作为预处理可明显提高反硝化速率,碳源脱氮率均在96%以上(树皮除外)。2种处理方式中均有NO2--N累积,部分碳源释放NH4+-N并发生DNRA反应,树叶在2种处理中脱氮效果均较好。结合各碳源脱氮率、耗碳源量以及处理成本,选取基本处理的香樟叶作为最佳纤维素碳源。 相似文献