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581.
Xuan Zhang Zhongming Chen Hongli Wang Shuzhong He Daoming Huang 《Atmospheric environment (Oxford, England : 1994)》2009,43(29):4465-4471
The aqueous ozonolysis of α-pinene and β-pinene was conducted under simulated tropospheric conditions at different pHs and temperatures. Three kinds of products, peroxides, carbonyl compounds, and organic acids, were well characterized, and the detection of these products provides effective evidence for understanding the atmospheric aqueous reaction pathway. We have two interesting findings: (1) the unexpected formation of methacrolein (MACR), with a yield of ~40%, in the α-pinene–O3 aqueous reaction indicates a potentially new SOA formation pathway, because MACR is one of the important precursors of SOA; and (2) the surprisingly high yields of H2O2, ~60% for the α-pinene–O3 reaction and ~100% for the β-pinene–O3 reaction, indicates that H2O2 can be a significant contributor to the origin and transformation of oxidants in the atmosphere, especially in the humid regions. Moreover, we have determined the rate constant for aqueous reaction between MACR and H2O2 in pH 2 to 7 and obtained its upper limit as 0.13 M L?1 s?1. A mechanism concerning the formation of the species mentioned above is proposed, and it differs from that in the gas-phase reaction. We suggest that water plays a key role in the mechanism, by participating in the reactions as a direct reactant and by removing the excess energy of intermediates formed in the reactions. 相似文献
582.
Chromium(VI)-containing sorbents in the form of sludge or solid residue from treatment processes are often landfilled or used as fill materials, therefore the long-term stability of metal binding is important. The reduction of Cr(VI)–Cr(III) through heat treatment may be a useful detoxification method. After heating at 500, 900, 1000, and 1100 °C for 4 h, the transformation of chemical states of chromium on 105 °C-dried, 7.9% Cr(VI)-doped TiO2 powders was studied on the basis of surface area measurements, scanning electron microscopy (SEM) images, X-ray diffraction (XRD), and extended X-ray absorption fine structure (EXAFS) spectra. It was shown that Cr(VI) was reduced to Cr(III) in the Cr(VI)-doped samples after heating within 500–900 °C. The present results also suggested that the chromium octahedral was bridged to the titanium tetrahedral and was incorporated in TiO2 minerals formed after 1000 °C treatment. 相似文献
583.
Site selection is an important and necessary issue for waste management in fast-growing regions. Because of the complexity of waste management systems, the selection of the appropriate solid waste landfill site requires consideration of multiple alternative solutions and evaluation criteria. Based on actual conditions of the study area, we considered economic factors, calculated criteria weights using the analytical hierarchy process (AHP), and built a hierarchy model for solving the solid waste landfill site-selection problem in Beijing, China. A geographic information system (GIS) was used to manipulate and present spatial data. All maps are graded from 1 (lowest suitability) to 5 (highest suitability) using spatial information technologies. The candidate sites were determined by aggregation based on the criteria weights. The candidate sites are divided by ‘best’, ‘good’ and ‘unsuitable’ landfill areas. Best landfill areas represent optimal sites; good landfill areas can be used as back-up candidate sites. Our work offers a siting methodology and provides essential support for decision-makers in the assessment of waste management problems in Beijing and other rapidly developing cities in developing countries. 相似文献
584.
The hydrolysis/precipitation behaviors of Al3+, Al13 and Al30 under conditions typical for flocculation in water treatment were investigated by studying the particulates' size development, charge characteristics, chemical species and speciation transformation of coagulant hydrolysis precipitates. The optimal pH conditions for hydrolysis precipitates formation for AlCl3, PACAl13 and PACAl30 were 6.5–7.5, 8.5–9.5, and 7.5–9.5, respectively. The precipitates' formation rate increased with the increase in dosage, and the relative rates were AlCl3 ? PACAl30 > PACAl13. The precipitates' size increased when the dosage increased from 50 μM to 200 μM, but it decreased when the dosage increased to 800 μM. The Zeta potential of coagulant hydrolysis precipitates decreased with the increase in pH for the three coagulants. The iso-electric points of the freshly formed precipitates for AlCl3, PACAl13 and PACAl30 were 7.3, 9.6 and 9.2, respectively. The Zeta potentials of AlCl3 hydrolysis precipitates were lower than those of PACAl13 and PACAl30 when pH > 5.0. The Zeta potential of PACAl30 hydrolysis precipitates was higher than that of PACAl13 at the acidic side, but lower at the alkaline side. The dosage had no obvious effect on the Zeta potential of hydrolysis precipitates under fixed pH conditions. The increase in Zeta potential with the increase in dosage under uncontrolled pH conditions was due to the pH depression caused by coagulant addition. Al–Ferron research indicated that the hydrolysis precipitates of AlCl3 were composed of amorphous Al(OH)3 precipitates, but those of PACAl13 and PACAl30 were composed of aggregates of Al13 and Al30, respectively. Al3+ was the most un-stable species in coagulants, and its hydrolysis was remarkably influenced by solution pH. Al13 and Al30 species were very stable, and solution pH and aging had little effect on the chemical species of their hydrolysis products. The research method involving coagulant hydrolysis precipitates based on Al–Ferron reaction kinetics was studied in detail. The Al species classification based on complex reaction kinetic of hydrolysis precipitates and Ferron reagent was different from that measured in a conventional coagulant assay using the Al–Ferron method. The chemical composition of Ala, Alb and Alc depended on coagulant and solution pH. The Alb measured in the current case was different from Keggin Al13, and the high Alb content in the AlCl3 hydrolysis precipitates could not used as testimony that most of the Al3+ was converted to highly charged Al13 species during AlCl3 coagulation. 相似文献
585.
Diversity of Soil Nematodes in Areas Polluted with Heavy Metals and Polycyclic Aromatic Hydrocarbons (PAHs) in Lanzhou,China 总被引:1,自引:0,他引:1
This study investigated the soil nematode community structure along the Yellow River in the Lanzhou area of China, and analyzed
the impact of heavy metals (Cd, Pb, Cr, Cu, and Zn) and polycyclic aromatic hydrocarbons (PAHs) on the nematode community.
Soil samples from five locations (named A–E), which were chosen for soil analysis, showed significant differences in their
heavy metal content (p < 0.01), as well as in the variety of nematodes (up to 41 genera) and families (up to 20) that were present. The different
samples also differed significantly in the total PAH content (p < 0.05), as well as the six types of PAH present. Sites A–C showed the most severe contamination with heavy metals and PAHs;
these sites had the lowest abundance of fungivores and omnivore/predators, but the proportion of bacteriovores was the highest
(p < 0.05). Site E, in contrast, showed only minor pollution with heavy metals and PAHs, and it contained the highest abundance
of plant parasites (p < 0.05). Several nematode ecological indicators were found to correlate with concentration of soil pollutants at all the
sites tested: the maturity index (MI, in addition to plant parasites), plant parasite index (PPI), ΣMI (including all the
soil nematodes), Shannon-Wiener diversity index (H′′), and Wasilewska index (WI). Disturbance to the soil environment was more severe when MI, ΣMI, and H′ values were lower. The results of the study show that the abundance and structure of the soil nematode communities in the
sampling locations were strongly influenced by levels of heavy metals and PAHs in the soil. They also show that the diversity
index H′ and the maturity index can be valuable tools for assessing the impact of pollutants on nematodes. 相似文献
586.
An Interval-Parameter Waste-Load-Allocation Model for River Water Quality Management Under Uncertainty 总被引:1,自引:0,他引:1
A simulation-based interval quadratic waste load allocation (IQWLA) model was developed for supporting river water quality
management. A multi-segment simulation model was developed to generate water-quality transformation matrices and vectors under
steady-state river flow conditions. The established matrices and vectors were then used to establish the water-quality constraints
that were included in a water quality management model. Uncertainties associated with water quality parameters, cost functions,
and environmental guidelines were described as intervals. The cost functions of wastewater treatment units were expressed
in quadratic forms. A water-quality planning problem in the Changsha section of Xiangjiang River in China was used as a study
case to demonstrate applicability of the proposed method. The study results demonstrated that IQWLA model could effectively
communicate the interval-format uncertainties into optimization process, and generate inexact solutions that contain a spectrum
of potential wastewater treatment options. Decision alternatives can be generated by adjusting different combinations of the
decision variables within their solution intervals. The results are valuable for supporting local decision makers in generating
cost-effective water quality management strategies. 相似文献
587.
This paper develops a methodology of proper scale analysis for regional industry development, which can be used in industry planning with the consideration of regional resource capacities. In the face of different data sources and even data scarcity, alternative methods based on linear programming and quadratic programming algorithms for calculating the resource intensity factors are designed. Based on the empirical study of industrialization, initial scenarios of industry development were set. Using HSY algorithm, sensitive industries that may cause exceeding regional resource capacity can be identified, and the risk of exceeding can be predicted and expressed in probability. Furthermore, a proper scale range can be designed for these sensitive industries according to resource capacity. Taking the case of Dalian city in China, this paper estimated the regional urban development plan, various resources capacities were studied, and land resources were estimated to be the most critical resource for the city. The land resource depletion intensities of different industries are calculated by quadratic programming algorithm. Under the constraint of 427.56 km2 available industrial land resources, the electronic and power industries have the most significant impact on total land use, if the scale of power industry exceeds 1.27 billion USD, the probability of land resource capacity breakthrough will be 50%. 相似文献
588.
The octanol–air partition coefficients (KOA) for PBB15, PBB26, PBB31, PBB49, PBB103 and PBB153 were determined as a function of temperature using a gas chromatographic retention time technique with 1,1,1-trichloro-2,2-bis (4-chlorophenyl) ethane (p,p′-DDT) as a reference substance. The internal energies of phase change from octanol to air (ΔOAU) were calculated for the six compounds and were in the range from 74 to 116 kJ mol−1. Simple regression equations of log KOA versus relative retention times (RRTs) on gas chromatography (GC), and log KOA versus molecular connectivity indexes (MCI) were obtained, for which the correlation coefficients (r2) were greater than 0.985 at 283.15 K and 298.15 K. Thus the KOA values of the remaining PBBs can be predicted by using their RRTs and MCI according to these relationships. 相似文献
589.
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
590.
Qing Xie Jingwen Chen Jianping Shao Changer Chen Hongxia Zhao Ce Hao 《Chemosphere》2009,76(11):1486-1490
Photolysis of deca-bromodiphenyl ether (BDE-209) was investigated in tetrahydrofuran, dichloromethane, isopropanol, acetone, ethanol, methanol, acetonitrile and dimethylsulfoxide. Noticeable differences of the photolytic rates and quantum yields were found in the diverse solvents. Different to the previous deductions, hydrogen donating efficiency and electron donating efficiency of solvents were not the decisive factors for the photolytic rate in this study, which was proved by the fast photolysis of BDE-209 in CCl4, a solvent without hydrogen and difficult to donate electrons. Besides hydrogen addition process, intermolecular polymerization might occur during the photolysis. Density functional theory (DFT) calculation was performed to understand the molecular properties of BDE-209 in different solvents. The lowest singlet vertical excitation energy (Eex) and the average formal charge on Br () of BDE-209, reflecting the difficulty for the excitation of BDE-209 and for the departing of Br atom, respectively, were changed by the reaction fields formed by the different solvents. Eex and linearly correlated with the photolytic activity (log k). This study is helpful to better understand the photolytic behavior of BDE-209 in different media. 相似文献