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711.
将Fe^2 与邻菲啰啉的显色反应引入流动注射系统,用盐酸羟胺将Fe^3 预先还原,0~6μg/ml的Fe^2符合比耳定律,检测出限0.11μg/ml。0.25μg/mlFe^2 经5次测定的标准偏差为2.2%,进样频率为120次/h,回收率98.5~104%。对工业废水中铁的测定取得了满意的效果。 相似文献
712.
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714.
有机磷农药在土壤环境中的降解转化 总被引:19,自引:1,他引:19
有机磷农药是世界上应用最广泛的农药种类之一 ,它属于比较容易降解的、对环境污染较小的农药。从有机磷农药的性质出发 ,着重讨论了有机磷农药的水解、光解和微生物降解 ,这也是有机磷农药在土壤中的主要降解转化过程 相似文献
715.
Mei Li Yao Zhang Chenglei Pei Jinwen Zhang Chunlei Cheng Xiufeng Lian Mubai Chen Bo Huang Zhong Fu Zhen Zhou 《环境科学学报(英文版)》2023,35(2):806-822
The real-time detection of the mixing states of polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs in ambient particles is of great significance for analyzing the source, aging process, and health effects of PAHs and nitro-PAHs; yet there is still few effective technology to achieve this type of detection. In this study, 11 types of PAH and nitro-PAH standard samples were analyzed using a high performance-single particle aerosol mass spectrometer (HP-SPAMS) in lab studies. The identification principles ‘parent ions’ and ‘mass-to-charge (m/z) = 77’ of each compound were obtained in this study. It was found that different laser energies did not affect the identification of the parent ions. The comparative experiments of ambient atmospheric particles, cooking and biomass burning emitted particles with and without the addition of PAHs were conducted and ruled out the interferences from primary and secondary organics on the identification of PAHs. Besides, the reliability of the characteristic ions extraction method was evaluated through the comparative study of similarity algorithm and deep learning algorithm. In addition, the real PAH-containing particles from vehicle exhaust emissions and ambient particles were also analyzed. This study improves the ability of single particle mass spectrometry technology to detect PAHs and nitro-PAHs, and HP-SPAMS was superior to SPAMS for detecting single particles containing PAHs and nitro-PAHs. This study provides support for subsequent ambient observations to identify the characteristic spectrum of single particles containing PAHs and nitro-PAHs. 相似文献
716.
研究了超声场降解水溶液中叔丁醇的行为,并探讨了反应动力学模式。实验表明.在本实验条件下超声波降解叔丁醇能够达到较好的降解效果。叔丁醇的去除率随着超声辐射时间的延长而提高,在频率为20kHz、功率为1500W的超声场下,作用80min能够达到90%左右的去除率。反映体系的降解速率随着反应温度的提高而升高,随着初始浓度的增大而降低:反应体系的pH值对叔丁醇的降解率影响不大:溶液中溶解气体的种类对降解效果有一定影响。反应速率常数按照由快到慢的顺序为ko2〉k未作处理〉kN2。在一定的初始浓度条件下,超声波降解叔丁醇的反应符合假一级反应动力学模式。 相似文献
717.
经过对PH玻璃电极对比观测实验,总结其在日常观测中衰减变化规律,以及PH电极失效前所具有的特征;讨论了对现有PH观测数据进行修正的方法,并编著相关修正程序;分析日常存在的测量误差,提出提高观测精度的措施。 相似文献
718.
Biotreatment of H2S- and NH3-containing waste gases by co-immobilized cells biofilter 总被引:11,自引:0,他引:11
Gas mixture of H2S and NH3 in this study has been the focus in the research area concerning gases generated from the animal husbandry and the anaerobic wastewater lagoons used for their treatment. A specific microflora (mixture of Thiobacillus thioparus CH11 for H2S and Nitrosomonas europaea for NH3) was immobilized with Ca-alginate and packed inside a glass column to decompose H2S and NH3. The biofilter packed with co-immobilized cells was continuously supplied with H2S and NH3 gas mixtures of various ratios, and the removal efficiency, removal kinetics, and pressure drop in the biofilter was monitored. The results showed that the efficiency remained above 95% regardless of the ratios of H2S and NH3 used. The NH3 concentration has little effect on H2S removal efficiency, however, both high NH3 and H2S concentrations significantly suppress the NH3 removal. Through product analysis, we found that controlling the inlet ratio of the H2S/NH3 could prevent the biofilter from acidification, and, therefore, enhance the operational stability. Conclusions from bioaerosol analysis and pressure drop in the biofilter suggest that the immobilized cell technique creates less environmental impact and improves pure culture operational stability. The criteria for the biofilter operation to meet the current H2S and NH3 emission standards were also established. To reach Taiwan's current ambient air standards of H2S and NH3 (0.1 and 1 ppm, respectively), the maximum inlet concentrations should not exceed 58 ppm for H2S and 164 ppm for NH3, and the residence time be kept at 72 s. 相似文献
719.
Study on the kinetics of cerium(III) adsorption-desorption on different soils of China 总被引:1,自引:0,他引:1
The kinetics of Ce(III) adsorption-desorption on four typical soils in China has been studied by using the batch method with the radioactive nuclide 141Ce. Results indicated that Ce(III) adsorption was rapid and nearly finished in less than 0.5 min. Desorption procedure was about completed in 1-30 min in the tested soils. Ce(III) desorption equilibrium times vary with different soils. The amounts of Ce(III) desorption on different soils in the same time were different. The Elovich equation proved to be the best models for fitting the data of Ce(III) desorption reactions in fluvo-aquic soil and black soil; and the parabolic-diffusion equation was the best model in red earth and loess soil. 相似文献
720.
Tsai CH Huang YJ Chen JC Liao WT Fang GC 《Journal of the Air & Waste Management Association (1995)》2003,53(10):1225-1232
The traditional technologies for odor removal of thiol usually create either secondary pollution for scrubbing, adsorption, and absorption processes, or sulfur (S) poisoning for catalytic incineration. This study applied a laboratory-scale radio-frequency plasma reactor to destructive percentage-grade concentrations of odorous dimethyl sulfide (CH3SCH3, or DMS). Odor was diminished effectively via reforming DMS into mainly carbon disulfide (CS2) or sulfur dioxide (SO2). The removal efficiencies of DMS elevated significantly with a lower feeding concentration of DMS or a higher applied rf power. A greater inlet oxygen (O2)/DMS molar ratio slightly improved the removal efficiency. In an O2-free environment, DMS was converted primarily to CS2, methane (CH4), acetylene (C2H2), ethylene (C2H4), and hydrogen (H2), with traces of hydrogen sulfide (H2S), methyl mercaptan (CH3SH), and dimethyl disulfide. In an O2-containing environment, the species detected were SO2, CS2, carbonyl sulfide, carbon dioxide (CO2), CH4, C2H4, C2H2, H2, formaldehyde, and methanol. Differences in yield of products were functions of the amounts of added O2 and the applied power. This study provided useful information for gaining insight into the reaction pathways for the DMS dissociation and the formation of products in the plasmolysis and conversion processes. 相似文献