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161.
Different advanced oxidation processes (AOPs) were applied to the treatment of a real cotton-textile dyeing wastewater as a pre-oxidation step to enhance the biodegradability of the recalcitrant compounds, which can be further oxidized using a biological process. Tests were conducted on a lab-scale prototype using artificial solar radiation and at pilot scale with compound parabolic collectors using natural solar radiation. The cotton-textile dyeing wastewater presents a lilac color, with a maximum absorbance peak at 641 nm, alkaline pH (pH?=?8.2), moderate organic content (DOC?=?152 mg C L?1, COD?=?684 mg O2 L?1) and low-moderate biodegradability (40 % after 28 days in Zahn–Wellens test). All the tested processes contributed to an effective decolorization and mineralization, but the most efficient process was the solar-photo-Fenton with an optimum catalyst concentration of 60 mg Fe2+ L?1, leading to 98.5 % decolorization and 85.5 % mineralization after less than 0.1 and 5.8 kJUV L?1, respectively. In order to achieve a final wastewater with a COD below 250 mg O2 L?1 (discharge limit into water bodies imposed by the Portuguese Legislation-Portaria no. 423/97 of 25 June 1997), considering the combination of a solar-photo-Fenton reaction with a biological process, the phototreatment energy required is 0.5 kJUV L?1, consuming 7.5 mM hydrogen peroxide, resulting in 58.4 % of mineralization $ \left({t}_{30\mathrm{W}}=3.2\ \min; \overline{T}=30.7\ {}^{\circ}\mathrm{C};\overline{\mathrm{pH}}=2.80;{\overline{\mathrm{UV}}}_{G,n}={13\ \mathrm{W}\ \mathrm{m}}^{-2}\right). $   相似文献   
162.
Catechol is a highly toxic organic pollutant, usually abundant in the waste effluents of industrial processes and agricultural activities. The environmental sources of catechol include pesticides, wood preservatives, tanning lotion, cosmetic creams, dyes, and synthetic intermediates. Genotoxicity of catechol at a concentration range 5?×?10?1–5 mM was evaluated by applying random amplified polymorphic DNA (RAPD) and time-lapse DNA laddering tests using onion (Allium cepa) root cells as the assay system. RAPD analysis revealed polymorphisms in the nucleotidic sequence of DNA that reflected the genotoxic potential of catechol to provoke point mutations, or deletions, or chromosomal rearrangements. Time-lapse DNA laddering test provided evidence that catechol provoked DNA necrosis and apoptosis. Acridine orange/ethidium bromide staining could distinguish apoptotic from necrotic cells in root cells of A. cepa.  相似文献   
163.
The dynamic light scattering (DLS) technique can detect the concentration and size distribution of nanoscale particles in aqueous solutions by analyzing photon interactions. This study evaluated the applicability of using photon count rate data from DLS analyses for measuring levels of biogenic and manufactured nanoscale particles in wastewater. Statistical evaluations were performed using secondary wastewater effluent and a Malvern Zetasizer. Dynamic light scattering analyses were performed equally by two analysts over a period of two days using five dilutions and twelve replicates for each dilution. Linearity evaluation using the sixty sample analysis yielded a regression coefficient R(2) = 0.959. The accuracy analysis for various dilutions indicated a recovery of 100 ± 6%. Precision analyses indicated low variance coefficients for the impact of analysts, days, and within sample error. The variation by analysts was apparent only in the most diluted sample (intermediate precision ~12%), where the photon count rate was close to the instrument detection limit. The variation for different days was apparent in the two most concentrated samples, which indicated that wastewater samples must be analyzed for nanoscale particle measurement within the same day of collection. Upon addition of 10 mg l(-1) of nanosilica to wastewater effluent samples, the measured photon count rates were within 5% of the estimated values. The results indicated that photon count rate data can effectively complement various techniques currently available to detect nanoscale particles in wastewaters.  相似文献   
164.
Chemical-Looping Combustion (CLC) is an emerging technology for CO2 capture because separation of this gas from the other flue gas components is inherent to the process and thus no energy is expended for the separation. Natural or refinery gas can be used as gaseous fuels and they may contain different amounts of light hydrocarbons. This paper presents the combustion results obtained with a Cu-based oxygen carrier using mixtures of CH4 and light hydrocarbons (LHC) (C2H6 and C3H8) as fuel. The effect on combustion efficiency of the fuel reactor temperature, solid circulation flow rate and gas composition was studied in a continuous CLC plant (500 Wth). Full combustions were reached at 1073 and 1153 K working at oxygen to fuel ratios, ? higher than 1.5 and 1.2 respectively. Unburnt hydrocarbons were never detected at any experimental conditions at the fuel reactor outlet. Carbon formation can be avoided working at 1153 K or at ? values higher than 1.5 at 1073 K. After 30 h of continuous operation, the oxygen carrier exhibited an adequate behavior regarding attrition and agglomeration. It can be concluded that no special measures should be taken in a CLC process with Cu-based OC with respect to the presence of LHC in the fuel gas.  相似文献   
165.
Iron (Fe) and other trace elements such as Zn, Mn, Ni and Cu are known as key-factors in marine biogeochemical cycles. It is believed that ocean primary productivity blooms in iron deficient regions can be triggered by iron in aeolian dust. Up to now, scarce aerosol elemental composition, based on measurements over sea at the Western South Atlantic (WSA), exist. An association between the Patagonian semi-desert dust/Fe and chlorophyll-a variability at the Argentinean continental shelf is essentially inferred from models. We present here experimental data of Fe enriched aerosols over the WSA between latitudes 22°S–62°S, during 4 oceanographic campaigns between 2002 and 2005. These data allowed inferring the atmospheric Fe flux onto different latitudinal bands which varied from 30.4 to 1688 nmolFe m?2 day?1 (October 29th–November 15th, 2003); 5.83–1586 nmolFe m?2 day?1 (February 15th–March 6th, 2004) and 4.73–586 nmolFe m?2 day?1(October 21st–November 5th, 2005).  相似文献   
166.
Nitrous oxide (N?O) is a long-lived and potent greenhouse gas produced during microbial nitrification and denitrification. In developed countries, centralized water reclamation plants often use these processes for N removal before effluent is used for irrigation or discharged to surface water, thus making this treatment a potentially large source of N?O in urban areas. In the arid but densely populated southwestern United States, water reclamation for irrigation is an important alternative to long-distance water importation. We measured N?O concentrations and fluxes from several wastewater treatment processes in urban southern California. We found that N removal during water reclamation may lead to in situ N?O emission rates that are three or more times greater than traditional treatment processes (C oxidation only). In the water reclamation plants tested, N?O production was a greater percentage of total N removed (1.2%) than traditional treatment processes (C oxidation only) (0.4%). We also measured stable isotope ratios (δN and δO) of emitted N?O and found distinct δN signatures of N?O from denitrification (0.0 ± 4.0 ‰) and nitrification reactors (-24.5 ± 2.2 ‰), respectively. These isotope data confirm that both nitrification and denitrification contribute to N?O emissions within the same treatment plant. Our estimates indicate that N?O emissions from biological N removal for water reclamation may be several orders of magnitude greater than N?O emissions from agricultural activities in highly urbanized southern California. Our results suggest that wastewater treatment that includes biological nitrogen removal can significantly increase urban N?O emissions.  相似文献   
167.
Hexavalent chromium is frequently found in industrial effluents as a result of the industrial applications of this compound and its anti-corrosive features. However, hexavalent chromium is extremely toxic, and its discharge in water is regulated, with a maximum limit of 0.1 mg/L in accordance with legislation established by CONAMA-Brazil (no. 397, April 3, 2008). To achieve lower discharge values, it is necessary to reduce from Cr(VI) to Cr(III), which is less toxic, and an economic alternative involves biological removal of this compound. Residence time distributions (RTDs) were measured to evaluate the behavior of actual biofilter operation conditions in a biofilter flow. The medium residence time distributions used were 8 and 24 h (recommended by the legislation). To optimize this process, a central composite design was used, considering the initial chromium concentration and pH as the independent variables and the removal of hexavalent chromium as the response. The boundary curves and surface response showed optimal behavior at 3.94 mg/L [Cr(0)] and a pH of 6.2. The removal process of hexavalent chromium is mathematically described by the Michaelis-Menten kinetic model. This model appropriately represents the variation of chromium concentration along the bioreactor.  相似文献   
168.
QuickRisk is a quantitative risk assessment tool developed at the Health and Safety Laboratory for use in assessing societal risk around onshore major hazard installations to inform land-use planning decisions. It uses release scenario information, parameterised consequence models, weather data, and population data from the National Population Database (NPD).This paper describes enhancements to the NPD methodology to include workplace populations. It describes the novel numerical, graphical and geographical representations of societal risk produced by QuickRisk. FN data are analysed in terms of scenario FN curves and Delta PLL vs. N curves, where PLL is potential loss of life. The Delta PLL curves could be useful for comparison of FN curves against FN criterion lines or other FN data on a PLL basis. Geographical representations generated from PLL density maps show: the distribution of PLL dominating release scenarios or the percentage of risk contributed by the PLL-dominant release scenario, the maximum number of fatalities associated with the worst-case event, and the associated release scenario. Geographical representations are also generated of the maximum population that would meet a PLL density criterion, and the relative population change that would match a given PLL density criterion.These novel representations of societal risk could be useful for more effective communication between stakeholders on the risk levels in the vicinity of major hazard installations.  相似文献   
169.
This research was aimed at understanding the dynamics of the herbicides diuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea], imazapic [2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methylnicotinic acid] and isoxaflutole [5-cyclopropyl-4-(2-methanesulfonyl-4-trifluoromethyl benzoyl)isoxazole] in two soils of different physico-chemical properties. To accomplish such intent, several greenhouse experiments were run. The bioavailability of diuron (0; 1.6 and 3.2 kg ha? 1), imazapic (0; 98 and 122.5 g ha? 1) and isoxaflutole (0; 35 and 70 g ha? 1) was measured in samples from a sandy loam soil and a clay soil, by sowing a bioindicator (Brachiaria decumbens), at 0, 25, 50, 75 and 100 days after herbicides application (DAA). Diuron was very stable in clay soil, providing control equal to or higher than 92% of bioindicator, up to 100 DAA, as assumed by biomass accumulation. No differential effect was observed in sandy loam soil, even when 2x labeled rate were applied. Imazapic provided a short bioavailability in relation to B. decumbens, independent of rates applied. The persistence of isoxaflutole was longer in clay soil (28 to 30 days).  相似文献   
170.
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