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铁锰层状双氢氧化物的制备及其对废水中Sb(Ⅲ)的吸附行为 被引量:3
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作者 杨金辉 李聪 +3 位作者 谢水波 杨斌 魏柏 田追 《复合材料学报》 EI CAS CSCD 北大核心 2022年第8期3871-3881,共11页
为更好地处理水环境中的锑(Ⅲ)污染问题,本论文采用超声共沉淀法制备了铁锰层状双氢氧化物(Fe-Mn LDH),并研究初始pH、投加量、共存离子、吸附时间及温度等因素对Fe-Mn LDH去除废水中Sb(Ⅲ)的影响。通过SEM、EDS、XRD、XPS和FTIR等表征... 为更好地处理水环境中的锑(Ⅲ)污染问题,本论文采用超声共沉淀法制备了铁锰层状双氢氧化物(Fe-Mn LDH),并研究初始pH、投加量、共存离子、吸附时间及温度等因素对Fe-Mn LDH去除废水中Sb(Ⅲ)的影响。通过SEM、EDS、XRD、XPS和FTIR等表征手段对材料晶体结构、形貌、吸附机制等进行了表征及分析。结果表明,Fe-Mn LDH去除Sb(Ⅲ)的适宜条件为:pH=5、投加量为0.4 g/L、吸附时间150 min;在此条件下,在温度45℃时最大吸附量为77.39 mg/g。吸附过程符合拟二级动力学模型,Freundich吸附等温线模型能够很好地描述Fe-Mn LDH对Sb(Ⅲ)的吸附行为。Sb(Ⅲ)吸附去除机制主要为离子交换、配位络合和静电吸附。通过四次吸附-解析实验发现,Sb(Ⅲ)去除率在83.03%以上,表明Fe-Mn LDH具备处理与修复含Sb(Ⅲ)废水污染的潜力。 展开更多
关键词 铁锰层状双氢氧化物 共沉淀 吸附 含Sb(Ⅲ)废水 机制
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Comparative Study on Characteristics of P Fixation by Mn, Fe and Al 被引量:24
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作者 LUQIMING LIAOZHONGWEN 《Pedosphere》 SCIE CAS CSCD 1997年第4期325-330,共6页
An experiment was conducted to examine the role of Mn in P fixation through comparing with Al and Fe. Hydroxides and oxides of Al, Fe and Mn were prepared in lab under opened and closed conditions to react with phosph... An experiment was conducted to examine the role of Mn in P fixation through comparing with Al and Fe. Hydroxides and oxides of Al, Fe and Mn were prepared in lab under opened and closed conditions to react with phosphate. The newly formed Mn hydroxide showed the strongest P-fixing abilityl even several times higher than Fe hydroxide, but became the lowest rapidly due to ageing when exposed to air. Mn oxide showed the lowest p-fixing ability. Therefore, a sound consideration on P fixation should be based on both quantities and p-fixing abilities of the compounds of Fe, Al and Mn. The importance of Mn on P availability should receive more attention especially under oxidation-reduction dynamic conditions. 展开更多
关键词 AL FE MN phosphate fixation
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Fe-Si-Mn-Oxyhydroxide Encrustations on Basalts at East Pacific Rise near 13°N:An SEM-EDS Study 被引量:5
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作者 WANG Xiaoyuan ZENG Zhigang +3 位作者 QI Haiyan CHEN Shuai YIN Xuebo YANG Baoju 《Journal of Ocean University of China》 SCIE CAS 2014年第6期917-925,共9页
Fe-Si-Mn-oxyhydroxide encrustations at the East Pacific Rise (EPR) near 13°N were analyzed using the scanning electron microscope (SEM) with an energy dispersive spectrometer (EDS). These encrustations are ... Fe-Si-Mn-oxyhydroxide encrustations at the East Pacific Rise (EPR) near 13°N were analyzed using the scanning electron microscope (SEM) with an energy dispersive spectrometer (EDS). These encrustations are mainly composed of amorphous Fe- Si-Mn-oxyhydroxides forming laminated, spherical, porous aggregates with some biodetritus, anhydrite, nontronite, and feldspar particles. Anhydrite particles and nontronite crystals in the Fe-Si-Mn-oxyhydroxide encrustations imply that the Fe-Si-Mn-oxyhy- droxide may have formed under relatively low- to high-temperature hydrothermal conditions. The Fe-Si-Mn-oxyhydroxide encrusta- tions on pillow basalts are 1-2mm thick. The growth rate of ferromanganese crusts in the survey area suggests that these encrusta- tions are an unlikely result of hydrogenic deposition alone having a hydrothermal and (Fe/Mn ratio up to 7.7 and Fe/(Fe+Mn+A1) ratio exceeding 0.78) hydrogenic origin (0.22 Fe/Mn ratio close to the mean value of 0.7 for open-ocean seamount crusts). The varying Fe/Mn ratios indicate that the Fe-Si-Mn-oxyhydroxide encrustations have formed through several stages of seafloor hydrother- malism. It is suggested that, at the initial formation stage, dense Fe-Si-oxyhydroxides with low Mn content deposit from a relatively reducing hydrothermal fluid, and then the loose Fe-Si-Mn-oxyhydroxides deposit on the Fe-Si-oxyhydroxides. As the oxidation degree of hydrothermal fluid increases and Si-oxide is inhibited, Mn-oxide will precipitate with Fe-oxyhydroxides. 展开更多
关键词 East Pacific Rise Fe-Si-Mn encrustations origin pillow basalt
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地下水系统中砷活化的钼同位素地球化学指示 被引量:2
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作者 李梦娣 周炼 +2 位作者 王焰新 吴潇 王帅 《地球科学(中国地质大学学报)》 EI CAS CSCD 北大核心 2014年第1期99-107,共9页
砷在天然环境中的迁移富集与氧化还原状态密切相关.盆地环境地下水中砷的活化迁移机制主要为沉积物中铁/锰氢氧化物由氧化还原条件变化导致发生还原性溶解进而释放吸附在其表面的砷.钼及钼同位素为氧化还原环境的重要指示参数,且铁/锰... 砷在天然环境中的迁移富集与氧化还原状态密切相关.盆地环境地下水中砷的活化迁移机制主要为沉积物中铁/锰氢氧化物由氧化还原条件变化导致发生还原性溶解进而释放吸附在其表面的砷.钼及钼同位素为氧化还原环境的重要指示参数,且铁/锰氢氧化物对钼同位素分馏有着重要的控制作用.将地下水的钼同位素应用于砷的活化迁移规律研究.大同盆地地下水中钼同位素比值(δ98 Mo)范围为-0.12‰^+2.17‰,相比于淡水中钼同位素组成偏重.桑干河河水的δ98 Mo为+0.72‰,与文献报道的河水平均钼同位素比值+0.7‰相当.大同盆地地下水中δ98 Mo与硫化物之间存在正相关关系,表明MoFe-S复合物可能形成于特定条件下,并优先利用水溶液中轻的钼使地下水中δ98 Mo比值升高.砷浓度与钼浓度之间的微弱负相关以及砷浓度与钼同位素之间的正相关说明,Mo-Fe-S的形成过程可能与同环境中As-Fe-S的复合物的形成存在竞争关系,进而使得地下水中砷富集.地下水中相对偏高的δ98 Mo可能来源于铁的氢氧化物对溶液中轻的钼的吸附速率高于先前吸附在铁的氢氧化物的钼的释放,且铁的氢氧化物对水溶液中钼的再吸附这一循环过程会导致地下水中钼浓度降低及钼同位素比值的升高.钼同位素指示的循环性的铁的氢氧化物的还原溶解及再氧化过程对砷的富集也有重要影响. 展开更多
关键词 钼同位素 铁锰氢氧化物 氧化还原反应 地球化学 大同盆地
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Enrichment mechanisms of rare earth elements in marine hydrogenic ferromanganese crusts 被引量:16
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作者 JIANG XueJun1,2,LIN XueHui1,2,YAO De3,4 & GUO WeiDong5 1 Key Laboratory of Marine Oil and Gas Resources and Marine Environment,Ministry of Land and Resources,Qingdao 266071,China 2 Qingdao Institute of Marine Geology,China Geological Survey,Qingdao 266071,China +2 位作者 3 Institute of Resources and Environment,Shandong University of Technology,Zibo 255049,China 4 Institute of Oceanology,Chinese Academy of Sciences,Qingdao 266071,China 5 Department of Oceanography,Xiamen University,Xiamen 361005,China 《Science China Earth Sciences》 SCIE EI CAS 2011年第2期197-203,共7页
A series of selective extraction experiments were conducted on marine hydrogenic ferromanganese crusts from the seamount near the Line Island to investigate the distribution of rare earth elements (REEs) and the mec... A series of selective extraction experiments were conducted on marine hydrogenic ferromanganese crusts from the seamount near the Line Island to investigate the distribution of rare earth elements (REEs) and the mechanisms of combination between REEs and the hydrogenic ferromanganese crusts. The enrichment of REEs in hydrogenic ferromanganese crusts is attributed mainly to the mineral or oxide/hydroxide of the crust rather than the growth environment. The REEs are present mainly in amorphous ferric oxide/hydroxide rather than in 6-MnO2. Amorphous ferric oxide/hydroxide preferentially combines free REE3+, while 6-MnO2 combines the REE-carbonate complexes in modern seawater. The REEs in seawater are combined more strongly with amorphous ferric oxide/hydroxides than with 6-MnO2. The positive Ce anomaly in hydrogenic ferromanganese crusts results from the oxidation of soluble Ce3+ to insoluble Ce4+ by the actively soluble oxygen of the bottom current rather than by the oxidation of δ-MnO2. 展开更多
关键词 rare earth elements hydrogenic ferromanganese crust selective extraction experiment GEOCHEMISTRY combinationmechanism
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