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911.
912.
Part V—sorption of pharmaceuticals and personal care products 总被引:5,自引:0,他引:5
Background, aim, and scope Pharmaceuticals and personal care products (PPCPs) including antibiotics, endocrine-disrupting chemicals, and veterinary pharmaceuticals
are emerging pollutants, and their environmental risk was not emphasized until a decade ago. These compounds have been reported
to cause adverse impacts on wildlife and human. However, compared to the studies on hydrophobic organic contaminants (HOCs)
whose sorption characteristics is reviewed in Part IV of this review series, information on PPCPs is very limited. Thus, a
summary of recent research progress on PPCP sorption in soils or sediments is necessary to clarify research requirements and
directions.
Main features We reviewed the research progress on PPCP sorption in soils or sediments highlighting PPCP sorption different from that of
HOCs. Special function of humic substances (HSs) on PPCP behavior is summarized according to several features of PPCP–soil
or sediment interaction. In addition, we discussed the behavior of xenobiotic chemicals in a three-phase system (dissolved
organic matter (DOM)–mineral–water). The complexity of three-phase systems was also discussed.
Results Nonideal sorption of PPCPs in soils or sediments is generally reported, and PPCP sorption behavior is relatively a more complicated
process compared to HOC sorption, such as the contribution of inorganic fractions, fast degradation and metabolite sorption,
and species-specific sorption mechanism. Thus, mechanistic studies are urgently needed for a better understanding of their
environmental risk and for pollution control.
Discussion Recent research progress on nonideal sorption has not been incorporated into fate modeling of xenobiotic chemicals. A major
reason is the complexity of the three-phase system. First of all, lack of knowledge in describing DOM fractionation after
adsorption by mineral particles is one of the major restrictions for an accurate prediction of xenobiotic chemical behavior
in the presence of DOM. Secondly, no explicit mathematical relationship between HS chemical–physical properties, and their
sorption characteristics has been proposed. Last but not least, nonlinear interactions could exponentially increase the complexity
and uncertainties of environmental fate models for xenobiotics. Discussion on proper simplification of fate modeling in the
framework of nonlinear interactions is still unavailable.
Conclusions Although the methodologies and concepts for studying HOC environmental fate could be adopted for PPCP study, their differences
should be highly understood. Prediction of PPCP environmental behavior needs to combine contributions from various fractions
of soils or sediments and the sorption of their metabolites and different species.
Recommendations and perspectives More detailed studies on PPCP sorption in separated soil or sediment fractions are needed in order to propose a model predicting
PPCP sorption in soils or sediments based on soil or sediment properties. The information on sorption of PPCP metabolites
and species and the competition between them is still not enough to be incorporated into any predictive models. 相似文献
913.
Vinicius F. Farjalla André M. Amado Albert L. Suhett Frederico Meirelles-Pereira 《Environmental science and pollution research international》2009,16(5):531-538
Background, aim, and scope Dissolved humic substances (HS) usually comprise 50–80% of the dissolved organic carbon (DOC) in aquatic ecosystems. From
a trophic and biogeochemical perspective, HS has been considered to be highly refractory and is supposed to accumulate in
the water. The upsurge of the microbial loop paradigm and the studies on HS photo-degradation into labile DOC gave rise to
the belief that microbial processing of DOC should sustain aquatic food webs in humic waters. However, this has not been extensively
supported by the literature, since most HS and their photo-products are often oxidized by microbes through respiration in
most nutrient-poor humic waters. Here, we review basic concepts, classical studies, and recent data on bacterial and photo-degradation
of DOC, comparing the rates of these processes in highly humic ecosystems and other aquatic ecosystems.
Materials and methods We based our review on classical and recent findings from the fields of biogeochemistry and microbial ecology, highlighting
some odd results from highly humic Brazilian tropical lagoons, which can reach up to 160 mg C L−1.
Results and discussion Highly humic tropical lagoons showed proportionally lower bacterial production rates and higher bacterial respiration rates
(i.e., lower bacterial growth efficiency) than other lakes. Zooplankton showed similar δ13C to microalgae but not to humic DOC in these highly humic lagoons. Thus, the data reviewed here do not support the microbial
loop as an efficient matter transfer pathway in highly humic ecosystems, where it is supposed to play its major role.
In addition, we found that some tropical humic ecosystems presented the highest potential DOC photo-chemical mineralization
(PM) rates reported in the literature, exceeding up to threefold the rates reported for temperate humic ecosystems. We propose
that these atypically high PM rates are the result of a joint effect of the seasonal dynamics of allochthonous humic DOC input
to these ecosystems and the high sunlight incidence throughout the year. The sunlight action on DOC is positive to microbial
consumption in these highly humic lagoons, but little support is given to the enhancement of bacterial growth efficiency,
since the labile photo-chemical products are mostly respired by microbes in the nutrient-poor humic waters.
Conclusions HS may be an important source of energy for aquatic bacteria in humic waters, but it is probably not as important as a substrate
to bacterial growth and to aquatic food webs, since HS consumption is mostly channeled through microbial respiration. This
especially seems to be the case of humic-rich, nutrient-poor ecosystems, where the microbial loop was supposed to play its
major role. Highly humic ecosystems also present the highest PM rates reported in the literature. Finally, light and bacteria
can cooperate in order to enhance total carbon degradation in highly humic aquatic ecosystems but with limited effects on
aquatic food webs.
Recommendations and perspectives More detailed studies using C- and N-stable isotope techniques and modeling approaches are needed to better understand the
actual importance of HS to carbon cycling in highly humic waters. 相似文献
914.
Jan Bernd Barhorst Roland Kubiak 《Environmental science and pollution research international》2009,16(5):582-589
Background, aim and scope The use of sodium hypochlorite (HYP) in viticulture results in effluents which are contaminated with halogenated substances.
These disinfection by-products (DBPs) can be quantified as group parameter ‘adsorbable organic halogens’ (AOX) and have not
been determined in effluents of viticulture yet. The substances that are detected as AOX are unknown. The AOX can be composed
of harmless substances, but even toxic contaminants. Thus, it is impossible to assess ecological impacts. The aim of this
study is to determine the quantification of AOX and DBPs after the use of HYP. This will be helpful to reduce environmental
pollution by AOX.
Materials and methods The potential of HYP to generate AOX was determined in laboratory-scale experiments. Different model solutions were treated
with HYP according to disinfection processes in viticulture and conditions of AOX formation in effluents were simulated. AOX
were quantified using the flask-shaking method and identified DBPs were investigated by gas chromatography–mass spectrometry.
Results Treatment with HYP resulted in the formation of AOX. The percentage conversion of HYP to AOX was up to 11%. Most important
identified DBPs in viticulture are chloroform, dichloroacetic acid and trichloroacetaldehyde. In addition, the formation of
carbon tetrachloride (CT), 1,1,1-trichloropropanone, 2,4-dichlorobenzoic acid and 2-chloro-/2,4-dichlorophenylacetic acid
was investigated. It was demonstrated that reaction temperature, concentration of HYP and type of organic matter have important
influence on the formation of chlorinated DBPs.
Discussion The percentage conversion of HYP to AOX was similar to other published studies. Although a correlation of single compounds
and AOX is difficult, chloroform was the predominant AOX. Generation of the volatile chloroform should be avoided due to possible
adverse effects. The generation of dichloroacetic acid is of minor importance on account of biodegradation. Trichloroacetaldehyde
and 1,1,1-trichloropropanone are weak mutagens and their formation should be avoided.
Conclusions The generation of AOX and chlorinated DBPs can be minimised by reducing the concentrations of the organic materials in the
effluents. The removal of organic matter before disinfection results in a decreased formation of AOX. HYP is an effective
disinfectant; therefore, it should be used at low temperatures and concentrations to reduce the amount of AOX. If possible,
disinfection should be accomplished by the use of no chlorine-containing agents. By this means, negative influences of HYP
on the quality of wine can also be avoided.
Recommendations and perspectives Our results indicate that HYP has a high potential to form AOX in effluents of viticulture. The predominant by-products are
chloroform, dichloroacetic acid and trichloroacetaldehyde. In further research, wastewaters from a winery and the in- and
outflows of two sewage treatment plants were sampled during vintage and analysed. These results will be discussed in a following
paper. 相似文献
915.
916.
颗粒化序列间歇式活性污泥反应器工艺处理化粪池污水 总被引:1,自引:1,他引:0
在序列间歇式活性污泥反应器(SBR)中成功培养出适应化粪池污水水质的好氧颗粒污泥.并将其应用于化粪池污水的处理.在好氧颗粒污泥培养的第15天左右,SBR中开始出现细小的颗粒,然后微生物在其上繁殖生长使颗粒逐渐增大而成熟;在第24天时,SBR中絮状活性污泥已基本实现了颗粒化.培养出的好氧颗粒污泥对化粪池污水有稳定的处理效果,在进水完全为化粪池污水时,COD、NH_4~+-N、TN的平均去除率分别为77%、61%、47%.但是,由于化粪池污水COD较低,因此无法维持较高的生物量,在后期的稳定运行过程中MLSS始终维持在2 500 mg/L左右.好氧颗粒污泥的同步硝化反硝化作用是其稳定脱氮的保证. 相似文献
917.
城市污水处理厂第二沉淀池出水的污染物浓度较低,经过矿化及灭菌等深度处理后可以回用,从而减轻对淡水资源的需求。本实验采用溶胶-凝胶法制备了负载TiO2的浮石光催化剂,对城市污水处理厂第二沉淀池出水进行了矿化及灭菌处理研究。采用低压汞灯对处理水样照射2h,有机物降解率可以达到50%,灭菌效率达到100%。处理后的水可以作为农作物灌溉、城市绿化和娱乐用水。负载在浮石表面的TiO2薄膜经过10次的光催化循环实验后,没有明显破损,可以再次循环使用。TiO2浮石具有质轻、机械性能好和价格低等优点,该方法处理废水的适用浓度低,可以广泛应用于微污染水和城市污水处理厂出水的深度处理。 相似文献
918.
Removal of trace elements in three horizontal sub-surface flow constructed wetlands in the Czech Republic 总被引:1,自引:0,他引:1
Lenka Kröpfelová Jaroslav Švehla 《Environmental pollution (Barking, Essex : 1987)》2009,157(4):1186-1194
Between March 2006 and June 2008 removal of 34 trace elements was measured on a monthly basis at three horizontal-flow constructed wetlands in the Czech Republic designed to treat municipal wastewater. In general, the results indicated a very wide range of removal efficiencies among studied elements. The highest degree of removal (average of 90%) was found for aluminum. High average removal was also recorded for zinc (78%). Elements removed in the range of 50-75% were uranium, antimony, copper, lead, molybdenum, chromium, barium, iron and gallium. Removal of cadmium, tin, mercury, silver, selenium and nickel varied between 25 and 50%. Low retention (0-25%) was observed for vanadium, lithium, boron, cobalt and strontium. There were two elements (manganese and arsenic) for which average outflow concentrations were higher compared to inflow concentrations. Reduced manganese compounds are very soluble and therefore they are washed out under anaerobic conditions. 相似文献
919.
Jason A. Dittman James B. Shanley George R. Aiken Janet E. Towse 《Environmental pollution (Barking, Essex : 1987)》2009,157(6):1953-1956
Stream water samples were collected over a range of hydrologic and seasonal conditions at three forested watersheds in the northeastern USA. Samples were analyzed for dissolved total mercury (THgd), DOC concentration and DOC composition, and UV254 absorbance across the three sites over different seasons and flow conditions. Pooling data from all sites, we found a strong positive correlation of THgd to DOC (r2 = 0.87), but progressively stronger correlations of THgd with the hydrophobic acid fraction (HPOA) of DOC (r2 = 0.91) and with UV254 absorbance (r2 = 0.92). The strength of the UV254 absorbance-THgd relationship suggests that optical properties associated with dissolved organic matter may be excellent proxies for THgd concentration in these streams. Ease of sample collection and analysis, the potential application of in-situ optical sensors, and the possibility for intensive monitoring over the hydrograph make this an effective, inexpensive approach to estimate THgd flux in drainage waters. 相似文献
920.
Cr(Ⅵ)污染土壤的热解还原无害化处理 总被引:4,自引:2,他引:2
提出了用热解还原法对含铬土壤进行无害化处理的新技术,研究了热解温度、热解时间及土壤有机质对铬无害化处理的影响,分析了热解前后土壤中铬的元素形态的变化.同时还探讨了热解还原过程中Cr(Ⅵ)的无害化机制.结果表明,土壤中的有机质在热解还原过程中产生的挥发分对Cr(Ⅵ)的无害化起核心作用;在200~600℃范围内,Cr(Ⅵ)的还原量随着热解温度升高而增大,500.0℃最适合于经济有效地实现Cr(Ⅵ)的热解还原处理;Cr(Ⅵ)的热解还原过程较快.铬的形态分析结果表明,热解后可交换态和碳酸盐结合态铬量大大降低,大部分铬转化成了活性低的残渣态,极大地降低了铬的危害. 相似文献