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93.
SBBR同步硝化反硝化处理生活污水的影响因素 总被引:38,自引:1,他引:38
序批式生物膜反应器SBBR采用塑料鲍尔环填料,在有氧情况下用于处理实际生活污水.该反应器能很好地创造缺氧微环境,载体生物膜具有吸附储碳能力,出现了良好的同步硝化和反硝化现象.反应器中溶解氧浓度在较大的范围内(0.8~4.0 mg·L-1)能有效地实现同步硝化和反硝化.当溶解氧浓度大于4.0 mg·L-1后,TN容积去除率大幅下降,出水TN大幅上升.增加载体生物膜厚度有利于同步硝化和反硝化.进水浓度基本不影响脱氮的效率,但出水TN随进水浓度增加而升高,建议原水浓度高时可增加后续脱氮处理或减少进水量来满足出水要求.优化运行方法和参数后,SBBR连续运行的TN去除率可稳定在74%~82%. 相似文献
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95.
Liu Fuqiang Xia Mingfang Fei Zhenghao Chen Jinlong Li Aimin 《Frontiers of Environmental Science & Engineering in China》2007,1(1):73-78
Both bottle-point and column-feeding experiments involving different solutes and sorbents were carried out to investigate
the adsorption selectivity and separation performance of salicylic acid and 5-sulfosalicylic acid. Their adsorption isotherms
onto such hypercrosslinked polymeric adsorbents as NDA-100 and NDA-99 could be well described by the Freundlich equations
whose characteristics describe extrathermic and favorable adsorption processes. The adsorption towards NDA-100 mainly depended
on the π-π interaction, while that towards NDA-99 was extremely influenced by the static-electric interaction. Additionally,
the adsorptive capacity of salicylic acid on NDA-99 decreased while it increased on NDA-100 with the presence of 5-sulfosalicylic
acid in the adsorptive environment as the competitive component. Comparatively, the adsorption capacity of 5-sulfosalicylic
acid decreased on both resins with salicylic acid as the competitive component. In fact, the difference in the interaction
between adsorbent and adsorbate resulted in the straight antagonism on the effective adsorption sites on the adsorbent. In
conclusion, the adsorption selectivity of salicylic acid onto NDA-100 was obviously larger than that onto NDA-99 with the
existence of 5-sulfosalicylic acid in the adsorptive environment. A satisfactory separation and recovery of tested solutes
in aqueous phase could be foreseeably achieved by the sequencing adsorption technique involving NDA-100 as well as NDA-99.
Translated from Environmental Pollution & Control, 2005, 27(8): 570–574 [译自: 环境污染与防治] 相似文献
96.
大气环境质量综合评价加权灰色关联模型的建立与应用 总被引:1,自引:2,他引:1
利用灰色理论建立大气环境质量综合评价加权灰色关联模型 ,运用污染贡献率确定权重系数。与其它评价模型相比 ,加权灰色关联模型还具有排序功能 ,实例表明该模型是简便有效的 相似文献
97.
In the Kranzberg forest near Freising (Germany) a novel “Free-Air Canopy O3 Exposure” system has been employed for analysing O3-induced responses from sub-cellular to ecosystem levels that are relevant for carbon balance and CO2 demand of 60-year-old beech trees. The below-ground ectomycorrhizal community was studied in two-fold ambient O3 concentrations (five cores per sampling) and in a control plot with an ambient O3 concentration (four cores per sampling). Five samplings were taken throughout two vegetation seasons (2003 and 2004). Types
of ectomycorrhiza were determined by their morphological, anatomical and molecular characteristics and quantified by counting.
The total number of mycorrhizal fine roots was higher at the fumigated plot as compared with the control site. The numbers
of ectomycorrhizal types at the fumigated and control plots were 28 and 26, respectively. Cenococcum geophilum was present in all soil cores at all sampling times with a significant increase in abundance under ozone-fumigated trees.
Other mycorrhizal types present at higher abundance at the fumigated than at the control plot were identified as Russula densiflora, R. fellea, R. illota, Tuber puberulum, Lactarius sp. 2 and Russula sp. 2. Some mycorrhizal types were present exclusively at the fumigated plot (Fagirhiza fusca, F. setifera, Lactarius acris, Piceirhiza nigra and Russula sp. 1). A possible ecological role for the abundant types of ectomycorrhiza and their putative application in bio-indication
is discussed. 相似文献
98.
Stin OC Carnahan A Singh R Powell J Furuno JP Dorsey A Silbergeld E Williams HN Morris JG 《Environmental monitoring and assessment》2003,81(1-3):327-336
Molecular methods, including DNA probes, were used to identify and enumerate pathogenic Vibrio species in the Chesapeake Bay; our data indicated that Vibrio vulnificus exhibits seasonal fluctuations in number. Our work included a characterization of total microbial communities from the Bay; development of microarrays that identify and quantify the diversity of those communities; and observation of temporal changes in those communities. To identify members of the microbial community, we amplified the 16S rDNA gene from community DNA isolated from a biofilm sample collected from the Chesapeake Bay in February, 2000. The resultant 75 sequences were 95% or more similar to 7 species including two recently described Shewanella species, baltica and frigidimarina, that have not been previously isolated from the Chesapeake. When the genera of bacteria from biofilm after culturing are compared to those detected by subcloning amplified 16S fragments from community DNA, the cultured sample exhibited a strong bias. In oysters collected in February, the most common bacteria were previously unknown. Based on our 16S findings, we are developing microarrays to detect these and other microbial species in these estuarine communities. The microarrays will detect each species using four distinct loci, with the multiple loci serving as an internal control. The accuracy of the microarray will be measured using sentinel species such as Aeromonas species, Escherichia coli, and Vibrio vulnificus. Using microarrays, it should be possible to determine the annual fluctuations of bacterial species (culturable and non-culturable, pathogenic and non-pathogenic). The data may be applied to understanding patterns of environmental change; assessing the health of the Bay; and evaluating the risk of human illness associated with exposure to and ingestion of water and shellfish. 相似文献
99.
中度嗜盐菌Halomonas sp.BYS-1启动子的克隆和测序 总被引:3,自引:0,他引:3
提取了中度嗜盐菌Halomonassp.BYS1的基因组DNA,以甲基对硫磷水解酶基因(mpd)为报告基因,以启动子探针pUCmpd为载体,通过鸟枪法在E.coliDH5α中构建了BYS1的启动子文库.通过筛选获得了17个阳性克隆,编号为P1~P17.测定了阳性克隆的甲基对硫磷水解酶(MPH)活性,结果表明,P3中mpd基因的启动子活性最强,它的酶活高达2554.3U/mg,而P17中mpd基因的启动子活性最弱,它的酶活只有68.3U/mg.对P3、P8、P17克隆中的重组质粒的插入片段进行了测序和在线启动子预测.图4表1参17 相似文献
100.
采用水解酸化一序列式活性污泥法(HA-SBR法)相结合技术处理季戊四醇废水,试验结果表明:(进水CODCR为726-1800ml/L,出水CODCR小于100ml/L,CODCR去除率为88.1%-95.8%,出水能满足国家排放标准。 相似文献