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171.
Continuous monitoring of ambient non-methane hydrocarbons (NMHCs) by automated gas chromatographs equipped with flame ionization detection (termed in-situ GC/FID) with hourly data resolution was instated in ozone non-attainment areas throughout Taiwan. Performance of these on-site in-situ GCs was validated by manual flask sampling, as well as by in-lab gas chromatography/mass spectrometry (GC/MS) analysis. More than 50 VOCs from C2 to C11 were analyzed by both methods. Ninety flask samples were collected in series near an in-situ GC monitoring station in order to closely compare with the in-situ measurements. Both time-series and scatter plots from the two methods are displayed and discussed. It was found that over-simplified, un-humidified single-point calibration leading to surface loss was responsible for the bias in the in-situ method, resulting in greater error in accuracy as VOC volatility decreased. Although this over-estimate of the concentrations was found across all target VOCs, both methods were able to consistently capture the variability of ambient VOCs, with R2 values greater than 0.9 for most of the major VOCs.  相似文献   
172.
Carbonyls emitted from essential oils can affect the air quality when they are used in indoors, especially under poor ventilation conditions. Lavender, lemon, rose, rosemary, and tea tree oils were selected as typical and popular essential oils to investigate in terms of composition, thermal characteristics and fifteen carbonyl constituents. Based on thermogravimetric (TG) analysis, the activation energy was 7.6–8.3 kcal mol?1, the reaction order was in the range of 0.6–0.7 and the frequency factor was 360–2838 min?1. Formaldehyde, acetaldehyde, acetone, and propionaldehyde were the dominant carbonyl compounds, and their concentrations were 0.034–0.170 ppm. The emission factors of carbonyl compounds were 2.10–3.70 mg g?1, and acetone, propionaldehyde, acetaldehyde, and formaldehyde accounted for a high portion of the emission factor of carbonyl compounds in essential oil exhaust. Some unhealthy carbonyl species such as formaldehyde and valeraldehyde, were measured at low-temperature during the vaporization of essential oils, indicating a potential effect on indoor air quality and human health.  相似文献   
173.
Surface sediments and sediment cores collected at the Pearl River Estuary (PRE) and its surrounding coastal area were analysed for total metal concentrations, chemical partitioning, and Pb isotopic compositions. The distribution of Cu, Cr, Pb, and Zn demonstrated a typical diffusion pattern from the land to the direction of the sea. Two hotspots of trace metal contamination were located at the mixed zone between freshwater and marine waters. The enrichment of metals in the sediments could be attributed to the deposition of the dissolved and particulate trace metals in the water column at the estuarine area. The similar Pb isotopic signatures of the sediments at the PRE and its surrounding coastal area offered strong evidence that the PRE was a major source of trace metals to the adjacent coastal area. Slightly lower (206)Pb/(207)Pb ratios in the coastal sediments may indicate other inputs of Pb in addition to the PRE sources, including the inputs from Hong Kong and other parts of the region.  相似文献   
174.
Liao W  Liu HW  Chen HJ  Chang WY  Chiu KH  Wai CM 《Chemosphere》2011,82(4):573-580
Catalytic hydrogenation of polycyclic aromatic hydrocarbons (PAHs) with up to four fused benzene rings over high-density-polyethylene-stabilized palladium nanoparticles in supercritical carbon dioxide via in situ UV/Vis spectroscopy is presented. PAHs can be efficiently converted to saturated polycyclic hydrocarbons using this green technique under mild conditions at 20 MPa of CO2 containing 1 MPa of H2 at 40-50 °C. Kinetic studies based on in situ UV/Vis spectra of the CO2 phase reveal that the initial hydrogenation of a given PAH and the subsequent hydrogenations of its intermediates are pseudo-first-order. The hydrogenation rate of the latter is always much smaller than that of the former probably due to increasing steric hindrance introduced by the hydrogenated benzene rings of PAHs which impedes the adsorption process and hydrogen access to PAHs on catalyst surfaces.  相似文献   
175.
Over decades of economic development, China's industrialization has led to significant environmental issues due to unregulated discharges into air, water, and soil. As cities continue to expand (i.e., urbanization trend) and awareness/concerns about environmental pollution rises, many industrial facilities along the edge of or within the city boundaries have been relocated or closed. This urbanization trend leaves behind idled and abandoned land that is contaminated from the former industrial activities and unregulated discharges. China released its first nationwide soil quality survey in April 2014, and the survey suggests that soil conditions in China represent a significant challenge. China has encouraged local engineering firms to demonstrate soil treatment technologies through pilot‐scale studies, but the outcomes of many demonstrations have not been promising due to the lack of remediation experience and underdeveloped technical guidelines that are needed to guide the remediation processes. During the past decade, some local soil remediation experience has been established, but it is limited for certain technologies that address their primary contaminants of concern: heavy metals and persistent organic pollutants. In 2014, national technical guidelines were published regarding environmental investigation, risk assessment, monitoring, and remediation; however, regulations and funding systems are still underdeveloped. Thus, the remediation processes that should maximize economic and environmental benefits are not streamlined. This article provides an overview of the latest regulatory developments, remediation technologies applied, technology trends, and market opportunities in China. The provided information aims to allow international remediation practitioners to better understand and appreciate this unique and emerging remediation market, which is growing fast, and to highlight the importance of developing a sustainable model that not only provides for cleanup of the environment but also supports economic development. ©2015 Wiley Periodicals, Inc.  相似文献   
176.
Corporations often become potentially responsible parties (PRPs) at hazardous waste sites because of their past transportation or disposal of hazardous substances at such sites. Determining a PRP's potential liability for the assessment and cleanup of hazardous waste sites is a challenging effort and often results in disputes among other PRPs regarding appropriate allocation of response action costs to each party. Further, public companies have an obligation to report probable and reasonably estimable costs under Generally Accepted Accounting Principles (GAAP) for environmental liabilities at their current or prior hazardous waste sites. The first step in such an evaluation is to determine whether or not a PRP can extricate themselves from any association with the subject site or, alternatively, demonstrate de minimis status. This article describes the methods by which PRPs can extricate themselves from liability associated with response action costs at contaminated sites, including: evaluating a PRP's prior settlements or indemnifications with other PRPs; identifying insurance coverage or other financial assurance instruments for the disposal facility; and examining applicable statutes of limitations against when a PRP received notification from the regulatory agency. The article also presents a case study discussing how a PRP with a portfolio of 72 hazardous waste disposal sites was able to extricate itself from the majority of these sites, resulting in only four sites where the PRP was determined to be a PRP and where an associated allocable share was assigned. © 2014 Wiley Periodicals, Inc.  相似文献   
177.
The main purpose of this study was to monitor ambient air particulates and particulate-bound Hg (Hg[p]) compositions in different crops in the coastal zone in the Taichung, Taiwan, area at a sampling site during 2013 October to 2013 December. In addition, a direct mercury analyzer (DMA-80) was used to directly detect the concentration with measured results by the regression equation of Hg in the ambient air. The results indicated that: 1) the mean values of ambient air Hg(p) compositions in rice displayed no significant differences for weeks one, two, and three versus those of the other crops (white cabbage, Arden lettuce, and Gynura procumbens); 2) for white cabbage, the higher the humidity, the lower the average ambient air Hg(p) compositions that were obtained, a phenomenon that was also reflected on the crops of white cabbage and G. procumbens; 3) Arden lettuce displayed no significant differences in the leaf Hg(p) compositions during weeks one, two, and three; however, the stem portions displayed significant differences in Hg(p) compositions during weeks two and three; and 4) the Spearman statistical method showed the mean differences for ambient air Hg(p) at the Long-jing sampling site (coastal regions) with four different crops (rice, white cabbage, Arden lettuce, and Gynura) in central Taiwan. The results further revealed no significant differences in mean values.  相似文献   
178.
This study investigated the effects of various factors on the anaerobic degradation of nonylphenol (NP) in soil. The results show that the optimal pH for NP degradation was 7.0 and that the degradation rate was enhanced when the temperature was increased. The addition of compost enhanced NP degradation. The individual addition of the electron donors lactate, acetate, and pyruvate inhibited NP degradation. The high-to-low order of NP degradation rates under three anaerobic conditions was sulfate-reducing conditions > methanogenic conditions > nitrate-reducing conditions. The results show that sulfate-reducing bacteria, methanogen, and eubacteria are involved in the anaerobic degradation of NP, with sulfate-reducing bacteria being a major component of the soil. Of the anaerobic strains isolated from the soil samples, strain AT3 expressed the best ability to biodegrade NP.  相似文献   
179.
Liu XH  Wai KM  Wang Y  Zhou J  Li PH  Guo J  Xu PJ  Wang WX 《Chemosphere》2012,88(5):531-541
Totally 117 cloud/fog water samples were collected at the summit of Mt. Tai (1534 m a.s.l.)—the highest mountain in the Northern China Plain. The results were investigated by a combination of techniques including back trajectory model, regional air quality and dust storm models, satellite observations and Principal Component Analysis. Elemental concentrations were determined by Inductively Coupled Plasma Mass Spectrometry, with stringent quality control measures. Higher elemental concentrations were found at Mt. Tai compared with those reported by other overseas studies. The larger proportions and higher concentrations of toxic elements such as Pb and As in cloud/fog water compared with those in rainwater at Mt. Tai suggests higher potential hazards of cloud/fog water as a source of contamination in polluted areas to the ecosystem. Peak concentrations of trace elements were frequently observed during the onset of cloud/fog events when liquid water contents of cloud/fog water were usually low and large amount of pollutants were accumulated in the ambient air. Inverse relationship between elemental concentrations and liquid water contents were only found in the samples with high electrical conductivities and liquid water contents lower than 0.3 g m−3. Affected mainly by the emissions of steel industries and mining activities, air masses transported from south/southwest of Mt. Tai were frequently associated with higher elemental concentrations. The element Mn is attributed to play an important role in the acidity of cloud/fog water. The composition of cloud/fog water influenced by an Asian dust storm event was reported, which was seldom found in the literature.  相似文献   
180.
Wu BZ  Chen HY  Wang SJ  Wai CM  Liao W  Chiu K 《Chemosphere》2012,88(7):757-768
Technologies such as thermal, oxidative, reductive, and microbial methods for the remediation of polychlorinated biphenyls (PCBs) have previously been reviewed. Based on energy consumption, formation of PCDD/F, and remediation efficiency, reductive methods have emerged as being advantageous for remediation of PCBs. However, many new developments in this field have not been systematically reviewed. Therefore, reductive technologies published in the last decade related to remediation of PCBs will be reviewed here. Three categories, including catalytic hydrodechlorination with H2, Fe-based reductive dechlorination, and other reductive dechlorination methods (e.g., hydrogen-transfer dechlorination, base-catalyzed dechlorination, and sodium dispersion) are specifically reviewed. In addition, the advantages of each remediation technology are discussed. In this review, 108 articles are referenced.  相似文献   
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