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1.
Bunge Michael Khknen Mika A. Rmisch Winfried Opel Matthias Vogler Susanne Walkow Fred Salkinoja-Salonen Mirja Lechner Ute 《Environmental science and pollution research international》2007,14(1):3-10
Background, Aims and Scope Sediments of the Spittelwasser creek are highly polluted with organic compounds and heavy metals due to the discharge of untreated
waste waters from the industrial region of Bitterfeld-Wolfen, Germany over the course of more than one century. However, relatively
few data have been published about the chloroorganic contamination of the sediment. This paper reports on the content of different
(chloro)organic compounds with special emphasis on polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F), and chlorobenzenes. Existing concepts for the remediation of Spittelwasser sediment include
the investigation of natural attenuation processes, which largely depend on the presence of an intact microbial food web.
In order to gain more insight in terms of biological activity, we analyzed the capacity of sediment microflora to degrade
organic matter by measuring the activities of extracellular hydrolytic enzymes involved in the biogeochemical cycling of carbon,
nitrogen, phosphorus and sulfur. Furthermore, the detection of physiologically active bacteria in the sediment, particularly
of those known for their capability to reductively dehalogenate organochlorine compounds, illustrates the potential for intrinsic
bioremediation processes.
Methods PCDD/F and chlorobenzenes were analyzed by gas chromatography(GC)/mass spectrometry and GC/flame ionization detection, respectively.
The activities of hydrolytic enzymes were determined from freshly sampled sediment layers using 4-methylumbelliferyl (MUF)
or 7-amino-4-methylcoumarin-conjugated model compounds and kinetic fluorescence measurements. Physiologically active bacteria
from different sediment layers were microscopically visualized by fluorescence in situ hybridization (FISH). Specific bacteria were identified by 16S rRNA gene amplification and sequencing.
Results and Discussion The PCDD/F congener profile was dominated by dibenzofurans. In addition, the presence of specific tetra and pentachlorinated
dibenzofurans supported the assumption that extensive magnesium production was one possible source for the high contamination.
A range of other chloroorganic compounds, including several isomers of chlorobenzenes, hexachlorocyclohexane and 1,1,1-trichloro-2,2-bis
(p-chloro-phenyl)ethane (DDT), was present in the sediment. Activities of extracellular hydrolytic enzymes showed a strong
decrease in those sediment layers that were characterized by high contents of absorbable organic halogen (AOX), indicating
disturbed organic matter decay. Interestingly, an abnormal increase of cellulolytic enzyme activities below the organochlorine-rich
layers was observed, possibly caused by residual cellulose from discharges of sulfite pulping wastes. FISH revealed physiologically
active bacteria in most sediment layers from the surface down to the depth of about 60 cm, including members of Desulfitobacterium (D.) and Sulfurospirillum. The presence of D. dehalogenans was confirmed by its partial 16S rRNA gene sequence.
Conclusions Results of chemical sediment analyses demonstrated high loads of organochlorine compounds, particularly of PCDD/F. Several
years after stopping the waste water discharge to Spittelwasser creek, this sediment remains a main source for pollution of
the downstream river system by way of the ongoing mobilization of sediment during high floods. As indicated by our enzyme
activity measurements, the decomposition potential for organic matter is low in organochlorine-rich sediment layers. In contrast,
the comparably higher enzyme activities in less organochlorine-polluted sediment layers as well as the presence of physiologically
active bacteria suggest a considerable potential for natural attenuation.
Recommendations and Perspectives From our data we strongly recommend to explore the degradative capacity of sediment microorganisms and the limits for in situ activity towards specific sediment pollutants in more detail. This will give a sound basis for the integration of bioremediation
approaches into general concepts to reduce the risk that permanently radiates from this highly contaminated sediment.
Submission Editor: Dr. Henner Hollert (Henner.Hollert@urz.uniheidelberg.de) 相似文献
2.
本文研究了钴(Ⅱ)催化过氧化氢氧化苯基荧光酮的褪色反应,测定了反应级数和表观活化能,建立了测定痕量地的新方法。25℃时本法检出限为29×10-13g/ml,线性范围为0.04~2ng/10ml,催化反应表观活化能为56.15KJ/mol。该方法己用于维生素B12、人发和茶叶中痕量钴的测定.结果满意,相对标准偏差为2.4~3.4%。 相似文献
3.
高灵敏XRF测定废水中痕量砷 总被引:2,自引:0,他引:2
本文提出了在硫酸介质中,以锌粒还原产生氢化物,溴化铜溶液吸收,微孔滤膜过滤制成薄样,X射线荧光测定水中痕量砷的分析方法。 相似文献
4.
采用恒能量同步荧光法检测了龙岩市大气颗粒物样品中的多环芳烃(PAHs),比较了龙岩市区大气颗粒物中多环芳烃含量的差异以及不同季节对多环芳烃含量的影响,讨论了其分布规律及污染源。 相似文献
5.
6.
研究了表面活性剂(乳化剂OP)存在下,铁、邻菲罗啉、曙红的显色反应.该离子缔合物的最大吸收波长为545 nm,摩尔吸光系数为9.4×104 L·mol-1·cm-1,铁含量在0-0.4 mg/L内符合比耳定律.以自来水为基体进行铁的回收实验,回收率在99%以上. 相似文献
7.
对铜的 3条谱线 (2 49.2 nm、2 61 .4nm,3 2 4.8nm ) ,铅的 2条谱线 (2 83 .3 nm、2 1 7.0 1 nm )以及锌的 2条谱线(3 0 7.6nm、2 1 3 .9nm ) ,共 7条谱线的灵敏度、检测限、线性范围进行了归纳性总结 ,并对多种共存元素可能存在的干扰情况进行了研究 ,认为利用元素不同分析谱线的分析灵敏度差异 ,根据被测元素在样品消解液中含量 ,选择合适的谱线进行分析 ,既降低工作强度 ,又能获得满意结果 相似文献
8.
Toral MI Beattie A Santibañez C Richter P 《Environmental monitoring and assessment》2002,76(3):263-274
A first derivative spectrophotometric method has been developedfor the determination of parathion and p-nitrophenol in vegetabletissues. Ethanol was used as solvent for extracting the compoundsfrom the tissues and subsequently the samples were evaluated against a vegetable tissue blank, directly by derivative spectrophotometry. The simultaneous determination of these compounds can be carried out using the zero-crossing approach for parathion at 253.0 nm and for p-nitrophenol at 273.1 nm. In the samples each analyte was determined in the presence of one another in the ranges between 4.9 to 3883.5 g g-1 forparathion and 4.9 to 3285.3 g g-1 for p-nitrophenol.The detection limits (3) were found to be 1.5 and 1.4 g g-1 for parathion and p-nitrophenol, respectively. The relative standard deviations were in all instances less than1.8%. The proposed method was applied to the determination ofthe analytes in spiked leafs of corn. The results show a goodrecovery and they are in agreement with those obtained bypolarography. 相似文献
9.
10.
氢化物发生原子荧光法测定饮用水中的微量硒时。仪器条件和试剂的浓度选择很重要。本文对条件的最佳化进行了实验。并对方法的精密度、准确度和检出限进行了讨论。 相似文献