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961.
Hung PC  Lo WC  Chi KH  Chang SH  Chang MB 《Chemosphere》2011,82(1):72-77
A laboratory-scale multi-layer system was developed for the adsorption of PCDD/Fs from gas streams at various operating conditions, including gas flow rate, operating temperature and water vapor content. Excellent PCDD/F removal efficiency (>99.99%) was achieved with the multi-layer design with bead-shaped activated carbons (BACs). The PCDD/F removal efficiency achieved with the first layer adsorption bed decreased as the gas flow rate was increased due to the decrease of the gas retention time. The PCDD/F concentrations measured at the outlet of the third layer adsorption bed were all lower than 0.1 ng I-TEQ Nm−3. The PCDD/Fs desorbed from BAC were mainly lowly chlorinated congeners and the PCDD/F outlet concentrations increased as the operating temperature was increased. In addition, the results of pilot-scale experiment (real flue gases of an iron ore sintering plant) indicated that as the gas flow rate was controlled at 15 slpm, the removal efficiencies of PCDD/F congeners achieved with the multi-layer reactor with BAC were better than that in higher gas flow rate condition (20 slpm). Overall, the lab-scale and pilot-scale experiments indicated that PCDD/F removal achieved by multi-layer reactor with BAC strongly depended on the flow rate of the gas stream to be treated.  相似文献   
962.
Wang B  Xue M  Lv Y  Yang Y  Zhong J  Su Y  Wang R  Shen G  Wang X  Tao S 《Chemosphere》2011,83(11):1461-1466
Oral ingestion of contaminated soil is an important pathway of human exposure to hydrophobic organic contaminants (HOCs), particularly for children in developing countries. The mobilization potential of various contaminants from ingested soil is often characterized using an in vitro gastrointestinal model, based on the quantities of contaminants remaining in digestive fluid after digestion and separation. Recently, it was experimentally demonstrated that a large fraction of mobilized contaminants sorbed on the digested residue could be released if the dissolved fraction was removed by intestinal absorption. This hypothesis was further tested in this study. Soil spiked with dichlorodiphenyltrichloroethane and its metabolites (DDXs) and polycyclic aromatic hydrocarbons (PAHs) was digested using an in vitro gastrointestinal model. A human colon carcinoma cell line (Caco-2) was cultured in digestive fluid with or without soil residue (pre-equilibrated with the soil) for 2 h. A large proportion of the contaminants (37-68%) was sorbed on the digested residue. Without this residue, 66 ± 13% of DDXs and 73 ± 14% of PAHs dissolved in the fluid, as means and standard deviations, were absorbed by the cell monolayer after exposure. With both digestive fluid and residue, the sorbed fraction of PAHs and DDXs decreased by 38-92%, while the ratios of the cellular to the dissolved concentrations were 2.7-2.8 times higher than those without the residue. This supported the hypothesis that the cell absorption of dissolved HOCs induces desorption of the sorbed fraction from digestive residue, and the desorbed HOCs can be absorbed as well.  相似文献   
963.
Pan B  Tao S  Wu D  Zhang D  Peng H  Xing B 《Chemosphere》2011,84(11):1578-1583
The sorption coefficients obtained in field investigation vary greatly from laboratory sorption experiments. The possible reasons were discussed in literature. Observing the commonly reported desorption hysteresis, this study proposed that the unclear sorption history of the field study could also result in the diverse sorption coefficients. This study conducted a comparative study regarding phenanthrene sorption/desorption behavior in low-concentration multi-time sorption process and the commonly applied high-concentration one-time sorption process. The sorption coefficients determined during the desorption process were much higher than those at sorption process. Thus, the prediction of sorption coefficient should be related with sorption history. Desorption hysteresis was increased with increased equilibration time and decreased solid-phase concentration. In addition, although the apparent contact time between sorbate and sorbent was shorter for low-concentration multi-time sorption, the desorption hysteresis was much stronger, which consequently result in higher sorption coefficients in comparison to high-concentration one-time sorption. Pore swelling or diffusion-controlled sorption kinetics could not explain this phenomenon. This study calls for research attention on sorption history, especially for field investigations.  相似文献   
964.
Bulk deposition samples were collected in remote, rural village and urban areas of Beijing-Tianjin region, North China in spring, summer, fall and winter from 2007 to 2008. The annually averaged PAHs concentration and deposition flux were 11.81 ± 4.61 μg/g and 5.2 ± 3.89 μg/m2/day respectively. PHE and FLA had the highest deposition flux, accounting for 35.3% and 20.7% of total deposition flux, respectively. More exposure risk from deposition existed in the fall for the local inhabitants. In addition, the PAHs deposition flux in rural villages (3.91 μg/m2/day) and urban areas (8.28 μg/m2/day) was 3.8 and 9.1 times higher than in background area (0.82 μg/m2/day), respectively. This spatial variation of deposition fluxes of PAHs was related to the PAHs emission sources, local population density and air concentration of PAHs, and the PAHs emission sources alone can explain 36%, 49%, 21% and 30% of the spatial variation in spring, summer, fall and winter, respectively.  相似文献   
965.
Bioaccessibility of organic pollutants in food is important for exposure estimation and risk assessment. An in vitro enzyme digestion experiment was carried out to analyze the bioaccessibility of PCBs in different foods including freshwater fish (bighead carp and oriental weather fish) and vegetables (spinach and cabbage). The results indicated that the bioaccessibility of PCBs in freshwater fish (3%) was much lower than that in leafy vegetables (25%). Based on field survey, the daily exposure TEQ value from these two types of food was 17.9 pg/kg bw/day. However, when bioaccessibility was taken into consideration, the value decreased to 0.61 pg/kg bw/day. Therefore, the forms of PCBs existing in food strongly influenced the bioavailability for humans, which may have important implications on dietary exposure. To our knowledge, this is the first paper to illustrate the bioaccessibility of PCBs in different foods using an in vitro digestion method.  相似文献   
966.
Yang CC  Chang SH  Hong BZ  Chi KH  Chang MB 《Chemosphere》2008,73(6):890-895
Development of effective PCDD/F (polychlorinated dibenzo-p-dioxin and dibenzofuran) control technologies is essential for environmental engineers and researchers. In this study, a PCDD/F-containing gas stream generating system was developed to investigate the efficiency and effectiveness of innovative PCDD/F control technologies. The system designed and constructed can stably generate the gas stream with the PCDD/F concentration ranging from 1.0 to 100ng TEQ Nm(-3) while reproducibility test indicates that the PCDD/F recovery efficiencies are between 93% and 112%. This new PCDD/F-containing gas stream generating device is first applied in the investigation of the catalytic PCDD/F control technology. The catalytic decomposition of PCDD/Fs was evaluated with two types of commercial V(2)O(5)-WO(3)/TiO(2)-based catalysts (catalyst A and catalyst B) at controlled temperature, water vapor content, and space velocity. 84% and 91% PCDD/F destruction efficiencies are achieved with catalysts A and B, respectively, at 280 degrees C with the space velocity of 5000h(-1). The results also indicate that the presence of water vapor inhibits PCDD/F decomposition due to its competition with PCDD/F molecules for adsorption on the active vanadia sites for both catalysts. In addition, this study combined integral reaction and Mars-Van Krevelen model to calculate the activation energies of OCDD and OCDF decomposition. The activation energies of OCDD and OCDF decomposition via catalysis are calculated as 24.8kJmol(-1) and 25.2kJmol(-1), respectively.  相似文献   
967.
采用浸渍法制备了Ca(Ⅱ)-AgNbO3光催化剂,并运用XRD、FT-IR、DRS、XPS和SEM对催化剂进行表征和分析.实验以亚甲基蓝为模拟污染物,在紫外光下考察Cu(Ⅱ)掺杂对AgNbO3光催化效果的影响.分析显示,掺杂Cu(Ⅱ)后AgNbO3晶型及表面形貌没有发生变化,但在可见光区的吸光度得到有效提高.光催化脱色结果表明,当Cu(Ⅱ)的掺杂量为2%(质量比),热处理温度为300℃,催化剂用量为1 g/L,亚甲基蓝初始浓度为10 mg/L,溶液pH值为7.15时,Cu(Ⅱ)-AgNbO3紫外光催化亚甲基蓝脱色的效果最好,3 h后,亚甲基蓝脱色率可达97.1%.  相似文献   
968.
汶川8.0级地震陕西强震台网数据记录的初步分析   总被引:1,自引:0,他引:1  
介绍了陕西数字强震动台网的组成及主要功能,对该台网汶川8.0级大震及其序列的记录数据进行了分析处理,在此基础上进行了陕西省地震烈度划分,进行了陕西关中地区地震烈度衰减关系的初步研究.  相似文献   
969.
Residual antibiotics in manure pose a potential threat to public and ecological health as a result of the application of manure from animals treated with antibiotics to land. The environmental fate of sulfonamides (SAs) in swine manure after composting and field application remains largely unknown. We studied the degradation of the antibiotics sulfadiazine (SD), sulfathiazole (ST), and sulfamethazine (SM2) during anaerobic composting. We tested the effects of temperature and antibiotic concentration on degradation rates. We also evaluated the changes in pH, moisture, and biological degradation material in manure spiked with SAs and in a control. Results showed that the 3 SAs decreased by between 52.31% and 90.30% in all 9 treatments following 14 days of anaerobic composting, and the highest removal efficiencies were observed at a temperature of 35°C and initial concentrations of 6.03, 6.48, and 6.32?µg/g of SD, ST, and SM2, respectively, which were degraded by 90.30%, 85.78%, and 75.18%. Removal efficiencies for all SAs correlated well with moisture and biological degradation material of the manure. These results indicate that composting may be a practical and effective way to reduce concentrations of these three SAs in swine manure prior to its land application.  相似文献   
970.
采用膜分离—变压吸附耦合工艺处理DQ催化剂载体生产过程产生的高浓度挥发性有机物(VOCs)废气。实验结果表明:在进气正己烷和非甲烷总烃的质量浓度分别为95 000~212 000 mg/m3和100 000 ~220 000 mg/m3、渗余侧压力0.25 MPa、渗透侧真空度0.09 MPa、进气流量15 Nm³/h的条件下,膜分离单元对废气中正己烷及非甲烷总烃的平均去除率分别为97.88%和97.29%;变压吸附单元对正己烷及非甲烷总烃的平均去除率分别为99.35%和99.33%;整套装置对正己烷及非甲烷总烃的平均总去除率分别为99.99%和99.98%。平均正己烷回收率达95.56%。处理后废气中非甲烷总烃质量浓度小于70 mg/ m3,达到北京市DB 11/ 447—2007 《炼油与石油化学工业大气污染物排放标准》的一级指标。  相似文献   
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