全文获取类型
收费全文 | 1875篇 |
免费 | 21篇 |
国内免费 | 15篇 |
专业分类
安全科学 | 46篇 |
废物处理 | 63篇 |
环保管理 | 265篇 |
综合类 | 415篇 |
基础理论 | 364篇 |
环境理论 | 1篇 |
污染及防治 | 535篇 |
评价与监测 | 96篇 |
社会与环境 | 112篇 |
灾害及防治 | 14篇 |
出版年
2023年 | 21篇 |
2022年 | 19篇 |
2021年 | 33篇 |
2020年 | 25篇 |
2019年 | 29篇 |
2018年 | 48篇 |
2017年 | 50篇 |
2016年 | 61篇 |
2015年 | 72篇 |
2014年 | 76篇 |
2013年 | 90篇 |
2012年 | 84篇 |
2011年 | 118篇 |
2010年 | 97篇 |
2009年 | 99篇 |
2008年 | 96篇 |
2007年 | 109篇 |
2006年 | 81篇 |
2005年 | 56篇 |
2004年 | 82篇 |
2003年 | 45篇 |
2002年 | 67篇 |
2001年 | 69篇 |
2000年 | 33篇 |
1999年 | 17篇 |
1998年 | 17篇 |
1997年 | 30篇 |
1996年 | 20篇 |
1995年 | 33篇 |
1994年 | 20篇 |
1993年 | 6篇 |
1992年 | 16篇 |
1991年 | 24篇 |
1990年 | 12篇 |
1989年 | 19篇 |
1988年 | 9篇 |
1987年 | 4篇 |
1985年 | 5篇 |
1984年 | 5篇 |
1982年 | 10篇 |
1981年 | 10篇 |
1979年 | 9篇 |
1970年 | 6篇 |
1969年 | 4篇 |
1966年 | 3篇 |
1965年 | 4篇 |
1962年 | 3篇 |
1960年 | 4篇 |
1959年 | 3篇 |
1954年 | 3篇 |
排序方式: 共有1911条查询结果,搜索用时 0 毫秒
51.
Bodar CW Berthault F de Bruijn JH van Leeuwen CJ Pronk ME Vermeire TG 《Chemosphere》2003,53(8):1039-1047
An evaluation was performed on the first group (41) of completed risk assessments for chemicals of the EU priority lists (Existing Chemicals; EC Regulation 793/93). The evaluation focussed on the conclusions of the risk assessments. The EU risk assessment process detected a high number of substances of concern. Furthermore priority chemicals may pose potential risks to the whole range of protection goals of the risk assessment. The predictability of the risk assessments for priority chemicals was investigated. Our a priori knowledge on possible risks of priority chemicals is found to be poor, especially for consumers. Both for environment and human health the potential risks were linked with a broad spectrum of use patterns. It is concluded that no industry category can in advance be excluded from performing risk assessments. For a great number of chemicals, additional testing was found to be needed to finalize the risk assessment. This evokes questions about the completeness of the current base-set, but also about the suitability of some of the submitted human health tests that should initially fulfil the base-set needs. The results of this evaluation are useful for ongoing discussions on risk assessment processes for chemicals. 相似文献
52.
Ghosh Shreya Gandhi Mayuri van Hullebusch Eric D. Das Alok Prasad 《Environmental science and pollution research international》2021,28(30):40249-40263
Environmental Science and Pollution Research - There has been alarming depletion of manganese (Mn) reserves owing to the ongoing extensive mining operations for catering the massive industrial... 相似文献
53.
54.
Social pressure on alluvial plains and deltas is large, both from an economic point of view and from a nature conservation point of view. Gradually, flood risks increase with economic development, because the expected damage increases, and with higher dikes, because the flooding depth increases. Global change, changing social desires, but also changing views, require a revision of flood-risk management strategies for the long term. These should be based on resilience as opposed to the resistence strategy of heightening dikes. Resilience strategies for flood-risk management imply that the river is allowed to temporarily flood large areas, whereas the flood damage is minimized by adapting land use. Such strategies are thus based on risk management and 'living with floods' instead of on hazard control. For The Netherlands, one of the most densely populated deltas in the world, alternative resilience strategies have been elaborated and assessed for their hydraulic functioning and 'sustainability criteria'. 相似文献
55.
This paper presents results of an experimental study into factors contributing to decay of odor samples during storage, between 4 and 40 hr after sample collection. The odor studied was sampled from a tobacco processing plant as part of collaborative research with a view to establishing a manual outlining methods for odor annoyance management, specifically for the tobacco industry. In August and September 1997, an experimental program was carried out in which two types of tobacco odor were sampled: Burley Toaster and Mix. The dependent variable was odor concentration in the bag, measured by dynamic olfactometry in accordance with the draft Comité Européen de Normalisation (CEN) standard EN13725 "Air Quality-Determination of Odor Concentration by Dynamic Olfactometry." The independent variables were sampling bag material, degree of dilution during sampling, dilution gas used, particle removal during sampling, and age of sample in hours. In the first phase, 94 odor analyses were carried out. In a second test, 32 samples were analyzed for odor concentration. In addition, 16 samples were analyzed using gas chromatography-mass spectrometry (GC-MS). Analysis of the results (analysis of variance) led to the unexpected conclusion that Nalophan film bags performed significantly better than metalized Cali-Bond layered film as a bag material. The odor concentration of samples in Nalophan bags remained relatively stable between 4 and 12 hr after sampling. After 30 hr, decay to about half the initial concentration, as measured at 4 hr, was observed. Particle removal during sampling caused the odor concentration in the bags to be reduced by approximately 20%. For practical reasons, particle removal remains useful, to avoid contamination of equipment. Using air or nitrogen as the neutral gas for pre-dilution during sampling or the dilution factor used (between factor 2 and 6) did not appear to have an effect on the decay characteristic of odor samples. The following recommendations are suggested for the practice of collecting odor samples and apply specifically to tobacco processing emissions: Analyze samples as soon as possible, preferably within 12 hr; When samples age for more than 12 hr, decay is likely to cause a reduction in odor concentration to half the original concentration at age 30 hr; Use sampling bags made of Nalophan NA or benchmark performance of other materials against Nalophan NA before using alternative materials; Use pre-dilution when sampling only for the purpose of avoiding condensation during sample storage. Use an appropriate minimum dilution factor to avoid condensation; Both nitrogen and high-purity (synthetic) air are suitable to use as neutral gas for pre-dilution; and When sampling tobacco odors, use an odorless filter to remove particles. This practice removes a source of variation and avoids contamination of equipment. The effect on results, despite being consistently lower in odor concentration, is not meaningful in terms of perceived intensity or annoyance potential. 相似文献
56.
van Eeden CM Liebenberg W du Preez JL de Villiers MM 《Journal of environmental science and health. Part. B》2004,39(1):33-51
In an effort to help with the development of effective dip vat management and waste disposal strategies this study determined how solution properties such as pH, buffer composition, ionic strength, temperature, solubility in organic solvents and the addition of commonly used solubilizing agents influenced the hydrolysis of amitraz. Amitraz degrade by means of hydrolysis described by a pseudo-first order rate process and a type ABCD pH rate profile. Hydrolysis increased with temperature and was fastest at low pH, slowest at neutral to slightly alkaline pH, and slightly increased above pH 10. However, buffer concentration and ionic strength influenced the hydrolysis rate and had to be accounted for before constructing a pH rate profile. Hydrolysis seems to depend on the dielectric constant of solvent mixtures and was fastest in water, slower in propylene glycol and ethanol solutions, and slowest in DMSO mixtures. In surfactant solutions, anionic micelles enhanced and cationic micelles retarded the hydrolysis rate. The magnitude of micellar effects decreased with increasing concentrations of the surfactants. The increased solubility and faster hydrolysis of amitraz in the sodium lauryl sulfate solutions showed that anionic surfactants potentially could be used for cleaning up amitraz spills, because it both solubilized the drug and catalyzed hydrolysis. 相似文献
57.
I. Vigano T. Rckmann R. Holzinger A. van Dijk F. Keppler M. Greule W.A. Brand H. Geilmann H. van Weelden 《Atmospheric environment (Oxford, England : 1994)》2009,43(35):5637-5646
Recent experiments have shown that dry and fresh leaves, other plant matter, as well as several structural plant components, emit methane upon irradiation with UV light. Here we present the source isotope signatures of the methane emitted from a range of dry natural plant leaves and structural compounds. UV-induced methane from organic matter is strongly depleted in both 13C and D compared to the bulk biomass. The isotopic content of plant methoxyl groups, which have been identified as important precursors of aerobic methane formation in plants, falls roughly halfway between the bulk and CH4 isotopic composition. C3 and C4/CAM plants show the well-established isotope difference in bulk 13C content. Our results show that they also emit CH4 with different δ13C value. Furthermore, δ13C of methoxyl groups in the plant material, and ester methoxyl groups only, show a similar difference between C3 and C4/CAM plants. The correlation between the δ13C of emitted CH4 and methoxyl groups implies that methoxyl groups are not the only source substrate of CH4.Interestingly, δD values of the emitted CH4 are also found to be different for C3 and C4 plants, although there is no significant difference in the bulk material. Bulk δD analyses may be compromised by a large reservoir of exchangeable hydrogen, but no significant δD difference is found either for the methoxyl groups, which do not contain exchangeable hydrogen. The δD difference in CH4 between C3 and C4 plants indicates that at least two different reservoirs are involved in CH4 emission. One of them is the OCH3 group, the other one must be significantly depleted, and contribute more to the emissions of C3 plants compared to C4 plants. In qualitative agreement with this hypothesis, CH4 emission rates are higher for C3 plants than for C4 plants. 相似文献
58.
BioDeNO(x), a novel technique to remove NO(x) from industrial flue gases, is based on absorption of gaseous nitric oxide into an aqueous Fe(II)EDTA(2-) solution, followed by the biological reduction of Fe(II)EDTA(2-) complexed NO to N(2). Besides NO reduction, high rate biological Fe(III)EDTA(-) reduction is a crucial factor for a succesful application of the BioDeNO(x) technology, as it determines the Fe(II)EDTA(2-) concentration in the scrubber liquor and thus the efficiency of NO removal from the gas phase. This paper investigates the mechanism and kinetics of biological Fe(III)EDTA(-) reduction by unadapted anaerobic methanogenic sludge and BioDeNO(x) reactor mixed liquor. The influence of different electron donors, electron mediating compounds and CaSO(3) on the Fe(III)EDTA(-) reduction rate was determined in batch experiments (21mM Fe(III)EDTA(-), 55 degrees C, pH 7.2+/-0.2). The Fe(III)EDTA(-) reduction rate depended on the type of electron donor, the highest rate (13.9mMh(-1)) was observed with glucose, followed by ethanol, acetate and hydrogen. Fe(III)EDTA(-) reduction occurred at a relatively slow (4.1mMh(-1)) rate with methanol as the electron donor. Small amounts (0.5mM) of sulfide, cysteine or elemental sulfur accelerated the Fe(III)EDTA(-) reduction. The amount of iron reduced significantly exceeded the amount that can be formed by the chemical reaction of sulfide with Fe(III)EDTA(-), suggesting that the Fe(III)EDTA(-) reduction was accelerated via an auto-catalytic process with an unidentified electron mediating compound, presumably polysulfides, formed out of the sulfur additives. Using ethanol as electron donor, the specific Fe(III)EDTA(-) reduction rate was linearly related to the amount of sulfide supplied. CaSO(3) (0.5-100mM) inhibited Fe(III)EDTA(-) reduction, probably because SO(3)(2-) scavenged the electron mediating compound. 相似文献
59.
60.
Juan M. González Benítez J. Neil Cape Mathew R. Heal Netty van Dijk Alberto Vidal Díez 《Atmospheric environment (Oxford, England : 1994)》2009,43(26):4087-4094
Water soluble organic nitrogen (WSON) compounds are ubiquitous in precipitation and in the planetary boundary layer, and therefore are a potential source of bioavailable reactive nitrogen. This paper examines weekly rain data over a period of 22 months from June 2005 to March 2007 collected in 2 types of rain collector (bulk deposition and “dry + wet” deposition) located in a semi-rural area 15 km southwest of Edinburgh, UK (N55°51′44″, W3°12′19″). Bulk deposition collectors are denoted in this paper as “standard rain gauges”, and they are the design used in the UK national network for monitoring precipitation composition. “Dry + wet” deposition collectors are flushing rain gauges and they are equipped with a rain detector (conductivity array), a spray nozzle, a 2-way valve and two independent bottles to collect funnel washings (dry deposition) and true wet deposition. On average, for the 27 weekly samples with 3 valid replicates for the 2 types of collectors, dissolved organic nitrogen (DON) represented 23% of the total dissolved nitrogen (TDN) in bulk deposition. Dry deposition of particles and gas on the funnel surface, rather than rain, contributed over half of all N-containing species (inorganic and organic). Some discrepancies were found between bulk rain gauges and flushing rain gauges, for deposition of both TDN and DON, suggesting biological conversion and loss of inorganic N in the flushing samplers. 相似文献