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11.
The conventional chemical reduction-precipitation technique in the removal of Cr(VI) from contaminated groundwater involves a two-step process whereby Cr(VI) is first reduced to Cr(III) at an acidic pH by a reducing agent and in a subsequent step, Cr(III) is precipitated as insoluble hydroxide at an alkaline pH. In a variation of this method, Fe(II) is added electrochemically to the Cr(VI) containing water. From a pure iron electrode, Fe(2+) ions are released into the solution and bring forth the reduction of Cr(VI). At the cathode, H(2)O is reduced whereby the OH(-) ions entering the solution keep the pH of the solution in the alkaline range. This latter fact greatly facilitates simultaneous reduction of Cr(VI) to Cr(III) and co-precipitation of hydroxides of trivalent Cr and Fe. On the basis of a set of experimental data, it is shown that this process is both thermodynamically and kinetically efficient, meaning, with the electrochemical method, rapid and nearly complete removal of Cr(VI) from a groundwater source with both high and low levels of Cr-contamination can be achieved. These factors make the electrochemical process superior to the conventional chemical process in remediation of Cr-contaminated groundwater. 相似文献
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Andreas Ahrens Arnim von Gleich und Lothar Li?ner 《Umweltwissenschaften und Schadstoff-Forschung》2002,14(3):165-169
Ohne Zusammenfassung
Online First: 27. 03. 2002
‚Sustainable Substitution of Hazardous Substances‚; Projektbeschreibung unter wwwoekopolde oder wwwfh-hamburgdelpers/gleich_von bzw. www.uni-hamburgde/kooperationssteI1e-hh. Das Vorhaben wird vom Bundesministerium für Bildung und Forschung (BMBF) im F?rderschwerpunkt ‚Rahmenbedingungen für Innovationen
zum nachhaitigen Wirtschaften’ (RIW) gef?rdert und von der GSF als Projekttr?ger betreut (FkZ. O7Riw4). 相似文献
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Hollert H Dürr M Holtey-Weber R Islinger M Brack W Färber H Erdinger L Braunbeck T 《Environmental science and pollution research international》2005,12(6):347-360
Goal, Scope and Background In order to evaluate the estrogenic activity of sediments and XAD water extracts of selected sites of the catchment area
of the River Neckar, a river system in Southern Germany, an integrative assessment approach was used to assess the ecological
hazard potential of endocrine-disrupting compounds in sediment and water.
Methods The approach is based on estrogen receptor-mediated vitellogenin synthesis induced in isolated hepatocytes of rainbow trout
and quantified in a non-radioactive dot blot/RNAse protection-assay in parallel to comprehensive chemical analyses of estrogenic
substances.
Results and Discussion Numerous investigated extracts revealed an estrogen activity comparable to that of the positive control (1 nM 17?-estradiol
corresponding to 270 ng/L in the test medium). Based on a concentration factor of 30 in the extracts and a recovery of XAD
resins of approximately 80 %, 17?-estradiol equivalent concentrations between 20 and 26.7 ng/L could be calculated downstream
of a sewage treatment plant (< 0.1 ng/L for a reference site). A comparison of the bioassay-derived Bio-TEQs (toxicity equivalents)
and the Chem-TEQs revealed a high correlation with a Pearson coefficient of 0.85, indicating that the same ranking of the
samples could be obtained with respect to the endocrine disrupting potential with both chemical and bioanalytical analysis.
However, the TEQ concentrations computed from chemical analyses were significantly lower than the bioassay-derived TEQ concentrations.
In fact, in none of the samples, more than 14 % of the vitellogenin-inducing potency could be attributed to the substances
(steroids, alkylphenols, bisphenol A, diethylstilbestrol) analyzed.
A comparison of the endocrine disrupting potential of sediments extracted by the solvents acetone and methanol revealed lower
biological effects for acetone-extracted samples. Possible reasons may be a masking of endocrine effects in acetone extracts
by cytotoxicity, a low extraction efficiency of the solvent acetone, or anti-estrogen potencies of some extracted sediment
compounds.
Using a mass balance approach, the contribution of the compounds analyzed chemically (Chem-TEQs) to the total endocrine activity
(Bio-TEQs) was calculated. Based on the very low detection limits, particularly of the steroids with their high TEF factors,
results revealed that a calculation of the Chem-TEQs is associated with considerable scale inaccuracy: Whereas only 7-15 %
of the biological effectiveness (Bio-TEQs) could be explained by endocrine substances identified above the detection limits,
the assumption of concentrations slightly below the given detection limits would result in a significant over estimation (137-197
%) of the Bio-TEQs. Even the interassay variation of the dot blot assay with different fish donors for primary hepatocyte
(factor 2 - 2.5) is relatively low, when compared to the large range of the Chem-TEQ concentrations (factor 20) obtained when
applying different modes of calculation.
Conclusions and Outlook Overall, only a minor portion of the endocrine activity detected by bioassays could be linked to compounds identified by
chemical analysis. In vitro assays for assessment of endocrine activities are useful as sensitive integrating methods that
provide quantitative estimates of the total activity of particular receptor-mediated responses. Although discrepancies may
also result from different bioanalytical approaches, it is overall likely that bioanalytical and not chemical analytical approaches
give the correct estimate of endocrine disrupting potencies in environmental samples. As a conclusion, assessment of endocrine
disruption based on chemical analysis alone does not appear sufficient and further research into the spectrum of substances
with potential endocrine activity as well as into additive or even synergistic effects in complex environmental samples is
urgently needed. 相似文献
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