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黄河断流成因及人文思考 总被引:2,自引:0,他引:2
日益严峻的黄河断流现象严重地影响了黄河流域经济和社会的可持续发展,也制约了西部大开发战略的实施。在分析了黄河断流的危害、成因的基础上,提出了在工程措施之外,要从人口、法律制度、产业结构等人文因素方面入手缓解黄河断流。 相似文献
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Yu Zhiang Ma Yuxia Zhang Yifan Cheng Bowen Feng Fengliu Ma Bingji Jiao Haoran Zhou Ji 《Environmental geochemistry and health》2021,43(10):4123-4138
Environmental Geochemistry and Health - Recently, particulate matter pollution has been worsening, which has been affecting the asthma visits in children. In this study, we assessed the short-term... 相似文献
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Haoran Feng Min Liu Wei Zeng Ying Chen 《Frontiers of Environmental Science & Engineering》2021,15(4):78
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Feng Zhang Shengsong Yu Jie Li Wenwei Li Hanqing Yu 《Frontiers of Environmental Science & Engineering》2016,10(3):531-538
Modification of electrode surface with carboxylic acid terminated alkanethiol self-assembled monolayers (SAMs) has been found to be an effective approach to improve the extracellular electron transfer (EET) of electrochemically active bacteria (EAB) on electrode surface, but the underlying mechanism behind such enhanced EET remains unclear. In this work, the gold electrodes modified by mercapto-acetic acid and mercaptoethylamine (Au-COOH, Au-NH2) were used as anodes in microbial electrolysis cells (MECs) inoculated with Geobacter sulfurreducens DL-1, and their electrochemical performance and the bacteria-electrode interactions were investigated. Results showed that the Fe(CN) 6 3–/4– redox reaction occurred on the Au-NH2 with a higher rate and a lower resistance than that on the Au or the Au-COOH. Both the MECs with the Au-COOH and Au-NH2 anodes exhibited a higher current density than that with a bare Au anode. The biofilm formed on the Au-COOH was denser than that on bare Au, while the biofilm on the Au-NH2 had a greater thickness, suggesting a critical role of direct EET in this system. This work suggests that functional groups such as–COOH and-NH2 could promote electrode performance by accelerating the direct EET of EAB on electrode surface. 相似文献
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In this study, stabilized Pd, Pt and Au nanoparticles were successfully prepared in aqueous phase using sodium carboxymethyl cellulose (CMC) as a capping agent. These metal nanoparticles were then tested for catalytic hydrodechlorination toward two classes of organochlorinated compounds (vinyl polychlorides including trichloroethylene (TCE), tetrachloroethylene (PCE), and alkyl polychlorides including 1,1,1-trichloroethane (1,1,1-TCA), and 1,1,1,2-tetrachloroethane (1,1,1,2-TeCA)) to determine the rate-limiting steps and to explore the reaction mechanisms. The surface area normalized reaction rate constant, kSA, showed a systematic dependence on the electronic structure (the density of states at the Fermi level) of the metals, suggesting that adsorption of organochlorinated reactants on the metal catalyst surfaces is the rate-limiting step for catalytic hydrodechlorination. Hydrodechlorination rates of 1,1,1-TCA and 1,1,1,2-TeCA agreed with the bond strength of the first (weakest) dissociated C-Cl bond, suggesting that C-Cl bond cleavage, which is the first step for dissociative adsorption of the alkyl polychlorides, controlled the catalytic hydrodechlorination rate. However, hydrodechlorination rates of TCE and PCE correlated with the adsorption energies of their molecular (non-dissociative) adsorption on the noble metals rather than with the first C-Cl bond strength, suggesting that molecular adsorption governs the reaction rate for hydrodechlorination of the vinyl polychlorides. 相似文献
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