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21.
对臭氧氧化去除焦化废水生化出水COD的反应动力学及其影响因素进行了实验研究,结果表明,在臭氧投加量为8.50mg/min,反应温度为20'E和初始pH为10.61条件下,对COD的降解符合表观一级反应动力学模型,其相关系数R。=0.9991,表观反应速率常数k。。=1.01×10^-3s-1。该条件下,臭氧氧化对COD的降解主要来源于高活性羟基自由基的强氧化作用。在不同的臭氧投加量(4.25~12.75mg/min)、不同的反应温度(10~40℃)和不同的初始pH(3.76~12.53)下,COD的降解也同样遵循一级反应动力学规律。随着臭氧投加量的增大,COD降解的表观反应速率常数从(0.554×10^-3)s-1增加到(1.06×10&-3)s-1;随着反应温度的升高,表观反应速率常数从(0.427×10^-3)s-1增加到(1.40×10-3)s-1,温度越高反应速率提高的幅度却越小;在初始pH3.76~10.61范围内,表观反应速率常数从(0.218×10^-3)s-1增加到(1.01×10^-3)s-1,在初始pH为12.53时表观反应速率常数下降到(0.857×10^-3)s-1。 相似文献
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The effects of turbulence intensity (velocity gradient, G (s−1)), Henry's law constant (H), and molecular weight (M) on the volatilization rates of organic compounds are examined using changes in the mass transfer coefficients (KOL (cm/min)) under specific liquid-mixing intensities. The selected compounds were divided into three groups according to their H values (mole in gas/mole in liquid, dimensionless), which ranged from 102 to 10−5. The relationship of the KOL relative to G, H and M was obtained via multiple regression. The obtained values of these parameters indicate that the primary factor affecting the KOL values of the high H compounds is their M values. The effects of the H values on the KOL values of the high H compounds can be neglected. On the other hand, the H value is the major factor determining the KOL values of the low H compounds. The changes in the KOL values of the different H compounds exhibit different profiles as the liquid-mixing intensity increases. The M and H values of middle H compounds possibly affect their KOL values. The effects of the liquid-mixing intensity on the KOL values of the organic compounds increase with increasing H values. The variation in the KOL values might be a result of the concentration of the organic compounds at the interface between the liquid and gas films. The empirical relationship between KOL and some selected parameters, G, H and M, is examined in this study. The obtained results can help to estimate volatilization loss of organic solutes in wastewater treatment facilities. 相似文献
24.
Jui-Pin Wu 《Chemistry and Ecology》2017,33(3):257-269
Although a freshwater planarian is proposed as a potential model for studying toxicities of environmental pollutants, they are less sensitive to metal exposures, compared to other freshwater invertebrates. We hypothesised that the metal uptake is low in treated planarians, which may lead to their higher tolerance to metals. The acute toxicities of Cu and Zn to Dugesia japonica were determined. The 24- and 48-h median lethal concentrations were 4.50 and 3.46?mg?L?1, respectively, for Cu, and 41.97 and 37.79?mg?L?1, respectively, for Zn. Accordingly, combining with the data on Cd in our previous study, higher tolerance of planarians to metals was revealed. Also, tissue levels of Cd, Cu, and Zn in treated D. japonica were determined, and their dissolved uptake rate constants (k1) were calculated. Results showed that bioaccumulations of these metals in D. japonica were, indeed, lower than that in other freshwater invertebrates having higher susceptibilities to these metals. 相似文献
25.
以地水中的氯代烃污染物三氯乙烯(TCE)为目标污染物,以过硫酸钾溶液为氧化剂,探讨了不同条件下过硫酸钾对TCE的去除效果。实验结果表明,在40℃,过硫酸钾初始浓度为2.43 g/L条件下,反应2 h后,TCE的去除率就可达到96.8%;过硫酸钾对TCE的去除符合一级反应动力学方程,速率常数(K)为1.3364 h-1,半衰期(t1/2)为0.51 h;过硫酸钾对TCE的去除速率在pH为中性附近时最大,其后无论pH升高或降低去除速率均减小;受温度和pH影响较明显,并且反应温度越高,受pH的影响越明显;随离子强度的增加而减小;反应活化能为119.6 kJ/mol;过硫酸钾溶于水生成过硫酸根离子(S2O28-),S2O28-会进一步生成硫酸根自由基(SO4-.),在碱性条件下,SO4-.与OH-反应会进一步生成羟基自由基(.OH)。过硫酸钾对于TCE的去除主要源自SO4-.和.OH的强氧化性。 相似文献
26.
The interactions between metals (Ca2+ and Hg2+) and extracellular polymeric substances (EPS) extracted from the aerobic and anaerobic sludge in wastewater treatment reactors were investigated using a combination of zeta potential measurement and 3-dimensional excitation–emission matrix (EEM) fluorescence spectroscopy with parallel factor (PARAFAC) analysis. Results show that Ca2+ had no substantial effects on the EEM fluorescence spectra of the EPS, but their zeta potentials increased with the increasing Ca2+ dosage. However, Hg2+ had a significant effect on the EEM fluorescence spectra of the EPS, while their zeta potentials seemed not to be affected by the dose of Hg2+. The interactions between Hg2+ and EPS were elucidated using the fluorescence quenching with PARAFAC analysis, while the interactions between Ca2+ and EPS were evaluated by the zeta potential technique. The binding constants for Hg2+ and EPS were two orders of magnitude higher than those for Ca2+ and EPS, suggesting that the binding mechanisms between Ca2+ and EPS were different from those between Hg2+ and EPS. The results might be useful for understanding the roles of EPS in bacterial self-protection against heavy metals and the aggregate formation mechanisms through ionic bridging interactions. 相似文献
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关于植物中氟化物测定结果的计算 总被引:1,自引:0,他引:1
针对植物中氟化物测定时由于绘制校准曲线的标准溶液体积与分析样品的定容体积不一样而引出的结果计算时的某些问题,提出了正确的计算方法和建议。 相似文献
29.
Sudha Rani Batchu Venkata R. Panditi Piero R. Gardinali 《Journal of environmental science and health. Part. B》2013,48(3):200-211
The photochemical fate of seven sulfonamides was investigated in matrices representative of natural water bodies under various light sources. Fundamental photolysis parameters such as molar absorption coefficient, quantum yield (QY) and first-order rate constants were determined. The photolysis decay rate was dependent on the protonation state of the molecule, pH of the water sample and dissolved organic matter. Natural organic matter was the most significant factor in the indirect photolysis of sulfonamides. Half-lives were in the range of minutes at 254 nm to days under natural sunlight. Under natural sunlight, all sulfonamides showed higher removal rates in natural waters implying that indirect photolysis is the predominant mechanism. 相似文献
30.
G. Bronzetti A. Galli P. Boccardo R. Vellosi R. Del Carratore E. Sabbioni 《毒物与环境化学》2013,95(1-2):103-111
The genotoxicity of chromium chloride was investigated in cells of D7 strain of Saccharomyces cerevisiae harvested either from logarithmic or stationary growth phase. A weak induction of mifotic gene conversion and point reverse mutation was obtained when the incubations were performed using phosphate buffer. No genetic effect was observed when the incubations were performed using Tris‐HCl buffer. The experiments with 51Cr radiotracer demonstrated that Cr3+ ion enters the yeast cells and binds to DNA even if the incubation mixture was performed with Tris HCl buffer. This behaviour could be due to the highest concentration of CrCl3 that cause some damages to cytoplasmatic membrane. 相似文献