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采用固相萃取-高效液相色谱-串联质谱法(SPE-HPLC-MS/MS)建立了地表水中25种抗生素类药物和8种非抗生素类药物的分析方法。通过重点优化质谱参数、色谱条件、样品pH、洗脱溶剂组成及用量等确定了最佳分析条件。水样经过滤、固相萃取柱富集净化后,选择Shim-pack XR-ODS为色谱柱,以乙腈和0.2%甲酸-2 mmol/L乙酸铵-水溶液为流动相进行梯度洗脱,采用电喷雾电离源,在多反应监测模式下(MRM)分析测定,内标法定量。33种药物的仪器定量限为0.012~4.68 ng/L,方法检出限为0.011~7.60 ng/L,地表水加标回收率为53.7%~122%,相对标准偏差为1.22%~32.1%(n=6)。方法成功应用于北京市凉水河12个地表水样分析,共检出32种药物,检出质量浓度为未检出~239 ng/L。利托那韦(RTV)作为新型冠状病毒诊疗方案中推荐的药物在凉水河检出率为100%。 相似文献
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TiO2 and montmorillonite composite photocatalysts were prepared and applied in degrading γ-hexachlorocyclohexane(γ-HCH)in soils.After being spiked with γ-HCH,soil samples loaded with the composite photocatalysts were exposed to UV-light irradiation.The results indicated that the photocatalytic activities of the composite photocatalysts varied with the content of TiO2 in the order of 10%<70%<50%<30%.Moreover,the photocatalytic activity of the composite photocatalysts with TiO2 content 30% was higher than that of the pure P25 with the same mass of TiO2.The strong adsorption capacity of the composite photocatalysts and quantum size effect may contribute to its increased photocatalytic activities.In addition,effect of dosage of composite photocatalysts and soil pH on γ-HCH photodegradation was investigated. Pentachlorocyclohexene,trichlorocyclohexene,and dichlorobenzene were detected as photodegradation intermediates,which were gradually degraded with tlle phOtOdegradation evolution. 相似文献
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天然水体中有机物检测方法的选择与优化 总被引:2,自引:0,他引:2
本文选取并优化了一种准确、易行、适合于天然水样中微量有机物的分析技术.天然水样品中有机物通过混合大孔径吸附树脂XAD-2与XAD-7(4:1,V/V)富集并用二氯甲烷洗脱.所有富集的有机物样品中均加入衍生化试剂N,O-双(三甲基硅基)三氟乙酰胺(缩写为BSTFA)硅烷化,最后采用气相色谱-质谱联用仪分析.为了实验的简便,我们的样品为模拟水样(4L添加定量5β-胆烷(挪威Chiron公司)的去离子水). 相似文献
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矿山嗣后充填法中,采用经验类比法判定胶结充填体的强度存在诸多问题。利用新的方法来分析充填体与岩体的匹配是必要的。对某铜矿灰砂比为1∶6、1∶8、1∶10和1∶12的4种尾砂胶结充填体进行力学试验和匹配分析。首先利用损伤力学方法建立充填体破坏前本构方程,根据岩体开挖释放能量与充填体蓄积应变能相近的原则,来判定岩体与充填体的匹配;然后运用GTS/MI-DAS有限元软件模拟开采-充填过程,根据应力变化与充填体极限强度的大小关系判定两者的匹配。2种方法所得到的结论一致。分析结果表明,该矿山宜采用充填配比不小于1∶10的尾砂胶结充填体。 相似文献
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Direct hydride derivatization of methyl- and ethylmercury chlorides in aqueous solution with KBH4 总被引:4,自引:0,他引:4
A convenient hydride derivatization procedure of methyl-and ethylmercury chlorides to volatile hydrides was reported. In sealed vials methylmercury and ethylmercury compounds in acidic aqueous solutions were converted into their volatile forms by the reaction with potassium tetrahydroborate(KBH4) and elvolved to the headspace of the vials. The gaseous analytes in the headspace were extracted and concentrated by solid phase microextraction(SPME) and injected into gas chromatography (GC) for separation and identified by mass selective detector(MS). 相似文献
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Naveen K. Shrivastava Shashikant B. Thombre Kailas L. Wasewar 《International Journal of Green Energy》2016,13(2):213-228
In order to understand the complex transport phenomena in a passive direct methanol fuel cell (DMFC), a theoretical model is essential. The analytical model provides a computationally efficient framework with a clear physical meaning. For this, a non-isothermal, analytical model for the passive DMFC has been developed in this study. The model considers the coupled heat and mass transport along with electrochemical reactions. The model is successfully validated with the experimental data. The model accurately describes the various species transport phenomena including methanol crossover and water crossover, heat transport phenomena, and efficiencies related to the passive DMFC. It suggests that the maximum real efficiency can be achieved by running the cell at low methanol feed concentration and moderate current density. The model also accurately predicts the effect of various operating and geometrical parameters on the cell performance such as methanol feed concentration, surrounding temperature, and polymer electrolyte membrane thickness. The model predictions are in accordance with the findings of the other researchers. The model is rapidly implementable and can be used in real-time simulation and control of the passive DMFC. This comprehensive model can be used for diagnostic purpose as well. 相似文献