全文获取类型
收费全文 | 5863篇 |
免费 | 601篇 |
国内免费 | 2879篇 |
专业分类
安全科学 | 322篇 |
废物处理 | 301篇 |
环保管理 | 1241篇 |
综合类 | 4730篇 |
基础理论 | 1167篇 |
污染及防治 | 993篇 |
评价与监测 | 422篇 |
社会与环境 | 126篇 |
灾害及防治 | 41篇 |
出版年
2024年 | 26篇 |
2023年 | 141篇 |
2022年 | 262篇 |
2021年 | 286篇 |
2020年 | 296篇 |
2019年 | 282篇 |
2018年 | 281篇 |
2017年 | 253篇 |
2016年 | 347篇 |
2015年 | 302篇 |
2014年 | 331篇 |
2013年 | 641篇 |
2012年 | 457篇 |
2011年 | 498篇 |
2010年 | 366篇 |
2009年 | 350篇 |
2008年 | 347篇 |
2007年 | 364篇 |
2006年 | 345篇 |
2005年 | 263篇 |
2004年 | 236篇 |
2003年 | 329篇 |
2002年 | 336篇 |
2001年 | 296篇 |
2000年 | 290篇 |
1999年 | 242篇 |
1998年 | 183篇 |
1997年 | 157篇 |
1996年 | 281篇 |
1995年 | 125篇 |
1994年 | 77篇 |
1993年 | 58篇 |
1992年 | 33篇 |
1991年 | 40篇 |
1990年 | 11篇 |
1989年 | 19篇 |
1988年 | 14篇 |
1987年 | 13篇 |
1986年 | 8篇 |
1985年 | 24篇 |
1984年 | 42篇 |
1983年 | 39篇 |
1982年 | 9篇 |
1981年 | 6篇 |
1980年 | 8篇 |
1978年 | 6篇 |
1977年 | 3篇 |
1972年 | 1篇 |
1971年 | 14篇 |
1967年 | 1篇 |
排序方式: 共有9343条查询结果,搜索用时 140 毫秒
381.
煤炭行业清费建税,资源税从价计征引起了社会各界对资源税费制度改革的热议,而资源耗减价值是资源税费制度改革的重要依据之一。将资源回采率纳入使用者成本模型,科学计量了我国2000-2011年间煤炭资源的耗减价值。分析表明:2000-2011年间,4%折现率下煤炭资源耗减价值增加了22倍之多,而资源税费却仅仅增长了7倍,煤炭资源耗减价值与资源税费实际征收额之间存在有巨大缺口得不到补偿;国家资源所有者权益的实现度与煤炭经济形势呈逆向分布,煤炭工业利润率的上升并没有带来国家资源所有者权益的增加,导致这种错位的原因与我国不合理的资源税收机制有很大关系;资源税税率的理论区间为1.11%-8.85%,与国家规定的2%-10%高度重合,从而说明国家决策的合理性。为使资源所有者权益的实现度与煤炭工业经济形势相"挂钩",以资源税收入等于资源耗减价值为切入点,对资源所有者权益的实现度进行数理分析,求得了资源税税率与当期资源价格的关系,发现固定税率的资源税难以适应市场波动,于是提出"资源税+利润税"的组合税收工具,确定了利润税的起征点,计算得出了资源税和利润税的税率组合。该组合税制在一定程度上能够平抑经济周期对煤炭工业造成的影响,同时又维护国家资源所有者权益,从而实现国家与煤炭工业"利益共享、风险共担"。 相似文献
382.
A majority of ongoing monitoring of persistent organic pollutants (POPs) is currently focused on chemicals emphasized in the Stockholm Convention. Quantitative detection of other substances (especially those with numerous anthropogenic sources such as polyaromatic hydrocarbons (PAHs)) is, however, also needed since their concentrations are usually several orders of magnitude higher. A goal of this study was to determine how various groups of compounds contribute to total human health risks at the variety of sampling sites in the region of Western Balkan. Distribution of the risks between the gas and particulate phases was also addressed. Results showed that inhalation exposure to organochlorine pesticides (OCPs) does not represent a significant risk to humans, while polychlorinated biphenyls (PCBs) re-volatilized to the atmosphere from contaminated soils and buildings can pose a problem. PCB evaporation from primary sources (currently used PCB-filled transformers or non-adequate storage facilities) generally resulted in much higher atmospheric concentrations than evaporation from the secondary sources (soils at the sites of war destructions). A majority of the human health risks at the urban sites were associated with PAHs. Between 83 and 94% of the cumulative risk at such sites was assigned to chemicals sorbed to particles, and out of it, PAHs were responsible for 99%. 相似文献
383.
J. R. Park M. J. Stabler P. J. Jones S. R. Mortimer J. R. Tiffin R. B. Tranter 《Environment, Development and Sustainability》2009,11(4):735-750
The issue of the sustainable development of rural economies in England has recently received considerable attention. This
is because many of the poorest areas in the country are rural, often of high environmental quality, but suffering from high
unemployment and a lack of services and facilities. The rapid decline in agricultural incomes and in-migration of affluent
urban workers since 1990 has exacerbated economic inequality in such areas. A number of factors have the potential to drive
rural development and this paper applies, and considers, the feasibility of a method from the USA for combining economic and
environmental variables in a regional growth model to examine the hypothesis that environmental quality is an important determinant
of sustainable rural development in England. The model output suggests that, although environmental quality does play a role
in sustainable rural development in England there are other, more important, factors driving development. These include business
and communications infra-structure, the degree and opportunities for commuting and underlying employment prospects. The robustness
and limitations of the method for combining economic and environmental variables is discussed in relation to the spatial interrelatedness
of Local Authority Districts in England, and conclusions are drawn about areas for refinement and improvement of the method.
相似文献
J. R. ParkEmail: |
384.
Plaza C Xing B Fernández JM Senesi N Polo A 《Environmental pollution (Barking, Essex : 1987)》2009,157(1):257-263
Binding of two model polycyclic aromatic hydrocarbons (PAHs), phenanthrene and pyrene, by humic acids (HAs) isolated from an organic substrate at different stages of composting and a soil was investigated using a batch fluorescence quenching method and the modified Freundlich model. With respect to soil HA, the organic substrate HA fractions were characterized by larger binding affinities for both phenanthrene and pyrene. Further, isotherm deviation from linearity was larger for soil HA than for organic substrate HAs, indicating a larger heterogeneity of binding sites in the former. The composting process decreased the binding affinity and increased the heterogeneity of binding sites of HAs. The changes undergone by the HA fraction during composting may be expected to contribute to facilitate microbial accessibility to PAHs. The results obtained also suggest that bioremediation of PAH-contaminated soils with matured compost, rather than with fresh organic amendments, may result in faster and more effective cleanup. 相似文献
385.
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
386.
铁炭微电解预处理电路板废水 总被引:3,自引:0,他引:3
采用铁炭微电解法预处理电路板废水.结果表明,在进水pH为2.00、铁炭质量比为4:1、振荡时间为20 min的铁炭微电解静态实验最佳条件下,絮凝出水COD去除率为30%;在进水pH为2.00、铁炭质量比为4:1、水力停留时间为50 min的铁炭微电解柱动态实验最佳条件下,连续曝气.絮凝出水COD为11021 mg/L,COD去除率约为34%,BOD5/COD从0.12上升到0.32,可生化性提高,Cu2+质量浓度从9.11 mg/L下降至0.76 mg/L,降低了废水的生物毒性,为生化处理创造了条件. 相似文献
387.
Gas/particle partitioning of atmospheric PCDD/Fs in a satellite town in Eastern China 总被引:3,自引:0,他引:3
Meng-xia Xu Jian-hua Yan Sheng-yong Lu Xiao-dong Li Tong Chen Ming-jiang Ni Hui-fen Dai Fei Wang Ke-fa Cen 《Chemosphere》2009,76(11):1540-1549
Gas/particle partitioning of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in ambient air was investigated in a satellite town in Eastern China from April 2007 to January 2008 comprehending large temperature variations (from 3 to 34 °C, daily average). Molecular weight, molecular structure and ambient temperatures are the three major factors that govern the gas/particle partitioning of atmospheric PCDD/Fs throughout the year. Generally, good agreements were obtained (except for winter) between measured particulate fractions and theoretical estimates of both the Junge–Pankow adsorption model and Harner Bidleman absorption model using different sets of subcooled liquid vapor pressure and octanol–air partition coefficient (Koa), respectively. Models utilizing estimates, derived from gas chromatographic retention indices (GC-RIs), are more accurate than that of entropy-based. Moreover, during winter, the Koa-based model using the GC-RIs approach performs better on lower chlorinated PCDD/Fs than that of -based. Furthermore, possible sources of mismatch between measured and predicted values in winter (3–7 °C) were discussed. Gas adsorption artifact was demonstrated to be of minor importance for the phenomena observed. On the other hand, large deviations of slopes (mr) and intercepts (br) in logKp vs. plots from theoretical values are observed in the literature data and these are found to be linearly correlated with ambient temperatures (P<0.001) in this study. This indicates that the non-equilibrium partitioning of PCDD/Fs in winter may be significantly influenced by the colder temperatures that may have slowed down the exchange between gaseous and particulate fractions. 相似文献
388.
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
389.
Long-range atmospheric transport of three toxaphene congeners across Europe. Modeling by chained single-box FATEMOD program 总被引:1,自引:1,他引:0
Jaakko Paasivirta Seija Sinkkonen Vladimir Nikiforov Fedor Kryuchkov Erkki Kolehmainen Katri Laihia Arto Valkonen Manu Lahtinen 《Environmental science and pollution research international》2009,16(2):191-205
Background, aims, and scope Since toxaphene (polychlorocamphene, polychloropinene, or strobane) mixtures were applied for massive insecticide use in the
1960s to replace the use of DDT, some of their congeners have been found at high latitudes far away from the usage areas.
Especially polychlorinated bornanes have demonstrated dominating congeners transported by air up to the Arctic areas. Environmental
fate modeling has been applied to monitor this phenomenon using parallel zones of atmosphere around the globe as interconnected
environments. These zones, shown in many meteorological maps, however, may not be the best way to configure atmospheric transport
in air trajectories. The latter could also be covered by connecting a chain of simple model boxes. We aim to study this alternative
approach by modeling the trajectory chain using catchment boxes of our FATEMOD model. Polychlorobornanes analyzed in biota
of the Barents Sea offered one case to study this modeling alternative, while toxaphene has been and partly still is used
massively at southern East Europe and around rivers flowing to the Aral Sea.
Materials and methods Pure model substances of three polychlorobornanes (toxaphene congeners P26, P50, and P62) were synthesized, their environmentally
important thermal properties measured by differential scanning calorimetry, as evaluated from literature data, and their temperature
dependences estimated by the QSPR programs VPLEST, WATSOLU, and TDLKOW. The evaluated property parameters were used to model
their atmospheric long-range transport from toxaphene heavy usage areas in Ukraine and Aral/SyrDarja/AmuDarja region areas,
through East Europe and Northern Norway (Finnmarken) to the Barents Sea. The time period used for the emission model was June
1997. Usual weather conditions in June were applied in the model, which was constructed by chaining FATEMOD model boxes of
the catchment’s areas along assumed maximal air flow trajectories. Analysis of the three chlorobornanes in toxaphene mixtures
function as a basis for the estimates of emission levels caused by its usage. High estimate (A) was taken from contents in
a Western product chlorocamphene and low estimate (B) from mean contents in Russian polychloroterpene products to achieve
modeled water concentrations. Bioaccumulation to analyzed lipid of aquatic biota at the target region was estimated by using
statistical calculation for persistent organic pollutants in literature.
Results The results from model runs A and B (high and low emission estimate) for levels in sea biota were compared to analysis results
of samples taken in August 1997 at Barents Sea. The model results (ng g−1 lw): 4–95 in lipid of planktovores and 7–150 in lipid of piscivores, were in fair agreement with the analysis results from
August 1997: 21–31 in Themisto libellula (chatka), 26–42 in Boreocadus saida (Polar cod), and 5–27 in Gadus morhua (cod) liver.
Discussion The modeling results indicate that the application of chained simple multimedia catchment boxes on predicted trajectory is
a useful method for estimation of volatile airborne persistent chemical exposures to biota in remote areas. For hazard assessment
of these pollutants, their properties, especially temperature dependences, must be estimated by a reasonable accuracy. That
can be achieved by using measurements in laboratory with pure model compounds and estimation of properties by thermodynamic
QSPR methods. The property parameters can be validated by comparing their values at an environmental temperature range with
measured or QSPR-estimated values derived by independent methods. The chained box method used for long-range air transport
modeling can be more suitable than global parallel zones modeling used earlier, provided that the main airflow trajectories
and properties of transported pollutants are predictable enough.
Conclusions Long-range air transport modeling of persistent, especially photo-resistant organic compounds using a chain of joint simple
boxes of catchment’s environments is a feasible method to predict concentrations of pollutants at the target area. This is
justified from model results compared with analytical measurements in Barents Sea biota in August 1997: three of six modeled
values were high and the other three low compared to the analysis results. The order of magnitude level was similar in both
modeled (planktovore and piscivore) and observed (chatka and polar cod) values of lipid samples. The obtained results were
too limited to firm validation but are sufficient to justify feasibility of the method, which prompts one to perform more
studies on this modeling system.
Recommendations and perspectives For assessment of the risk of environmental damages, chemical fate determination is an essential tool for chemical control,
e.g., for EU following the REACH rules. The present conclusion of applicability of the chained single-box multimedia modeling
can be validated by further studies using analyses of emissions and target biota in various other cases. To achieve useful
results, fate models built with databases having automatic steps for most calculations and outputs accessible to all chemical
control professionals are essential. Our FATEMOD program catchments at environments and compound properties listed in the
database represent a feasible tool for local, regional, and, according our present test results, for global exposure predictions.
As an extended use of model, emission estimates can be achieved by reversed modeling from analysis results of samples corresponding
to the target area.
This article is dedicated to the memory of Professor Alexander B Terentiev (who passed away in November 2006), our true friend.
With his Institute of Organo-Element Compounds, Russian Academy of Science, Moscow, he was an important main organizer of
the six joint Finnish–Russian seminars (every third year since 1989) on the field (‘Chemistry and Ecology of Organo-Element
Compounds’). He prompted us especially to search properties and environmental fates for various polyhalogen compounds. We
remember him for his friendly character and great sense of humor. 相似文献
390.
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