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利用红外气体箱式法(Infrared Gas Analyze,IRGA),于2008年8月晴天对福州市马尼拉草坪(Zoysia matrel-la)的生态系统CO2净交换(NEE)和环境因子进行观测,阐明NEE及其组分的昼夜动态变化特征和影响因子。马尼拉草坪NEE的昼夜变化呈现为单峰型曲线,昼间其变化规律较强,夜间呈波动状态。NEE(取绝对值)最大值出现在10:00,最小值出现在16:00左右。太阳辐射、腔室内空气相对湿度和气温与NEE的相关性均为极显著(p<0.01),太阳辐射、腔室内空气相对湿度和5cm土壤温度共同解释NEE速率昼夜变异的89.30%。太阳辐射和腔室内空气相对湿度是影响草坪生态系统CO2净交换量日动态的主导环境因子;其中,太阳辐射可以单独解释NEE速率昼夜变化的79.70%,腔室内空气相对湿度可以单独解释NEE速率昼夜变化的50.40%;夏季晴天草坪生态系统在日尺度上表现为净吸收,平均CO2净交换速率为-4.11μmol/(m2.s)(负值表示吸收),平均日总通量为-0.18 mol/(m2.d)。 相似文献
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Fluorescence excitation-emission spectroscopy with regional integration analysis for assessment of compost maturity 总被引:3,自引:0,他引:3
Composting of animal manures is believed as an alternative way for directly recycling them in farms, and therefore assessment of compost maturity is crucial for achieving high quality compost. Fluorescence excitation-emission matrices (EEMs) combined with regional integration analysis is presented to assess compost maturity. The results showed that the EEM contours of water-extract organic matter (WEOM) from immature composts exhibited four peaks at excitation/emission (Ex/Em) of 220/340 nm, 280/340 nm, 220/410 nm, and 330/410 nm, whereas EEM contour of WEOM from mature composts had only two peaks at Ex/Em of 230/420 nm and 330/420 nm. Pearson correlation demonstrated that peaks intensity rather than their ratios had a significantly correlation with the common indices assessing compost maturity, whereas the normalized excitation-emission area volumes (Φi,ns) from regional integration analysis had a stronger correlation with the common indices assessing compost maturity than peaks intensity. It is concluded that the Φi,ns from regional integration analysis are more suitable to assess the maturity of compost than the intensities of peaks. Therefore, the fluorescence spectroscopy combined with regional integration analysis can be used as a valuable industrial and research tool for assessing compost maturity, given its high sensitivity and selectivity. 相似文献
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Benn TM Westerhoff P Herckes P 《Environmental pollution (Barking, Essex : 1987)》2011,159(5):1334-1342
Detection methods are necessary to quantify fullerenes in commercial applications to provide potential exposure levels for future risk assessments of fullerene technologies. The fullerene concentrations of five cosmetic products were evaluated using liquid chromatography with mass spectrometry to separate and specifically detect C60 and C70 from interfering cosmetic substances (e.g., castor oil). A cosmetic formulation was characterized with transmission electron microscopy, which confirmed that polyvinylpyrrolidone encapsulated C60. Liquid-liquid extraction of fullerenes from control samples approached 100% while solid-phase and sonication in toluene extractions yielded recoveries of 27-42%. C60 was detected in four commercial cosmetics ranging from 0.04 to 1.1 μg/g, and C70 was qualitatively detected in two samples. A single-use quantity of cosmetic (0.5 g) may contain up to 0.6 μg of C60, demonstrating a pathway for human exposure. Steady-state modeling of fullerene adsorption to biosolids is used to discuss potential environmental releases from wastewater treatment systems. 相似文献
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As a result of the changes that occur during their use, used engine oils tend to differ in chemical and physical composition from a virgin oil. In general recycled oils have: much higher water and sediment levels than virgin oil; relatively higher concentrations of organic compounds (oxidation products); and relatively higher levels of metals such as Fe, Cd, Cr, Pb, etc. Therefore, the aim of this work was to investigate, assess and to observe, by means of the physical and the chemical properties of the oils, atomic absorption (AA), inductive couple plasma (ICP) and Fourier transform infrared (FTIR) analyses the extent of the differences occurring between the virgin and recycled oil. In important part of this work was also the development of analytical techniques based on the use of FTIR spectroscopy; in relation to the rapid analysis of lubricants; in particular for the differentiation of virgin and recycled oil. The results obtained were expected to be useful for differentiation purposes, providing information on whether the metal concentrations and oxidation products could be an appropriate feature for differentiating a particular oil sample from the others. This work is categorized into a two-step procedure. Firstly, an evaluation of a typical FTIR spectrum of an engine oil sample (mono- and multigrade) is presented. The broad feature centered at 1716 cm(-1) is due to the presence of carbonyl containing degradation products of oil. A band observed at 1732, 1169, 1154 and 1270 cm(-1) assigned to the polymethacrylate stretching vibrations, allows the determination of viscosity modifier and pour point depressant additives. The observed differences in the specific spectral bands (1732, 1169, 1154 and 1270 and 1716 cm(-1)) are investigated and discussed. Secondly, an analytical technique for the measurement of the levels of the wear metals is also applied. 相似文献