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Kinetics and corrosion products of aqueous nitrate reduction by iron powder without reaction conditions control 被引量:17
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作者 FAN Xiaomeng GUAN Xiaohong +1 位作者 MA Jun AI Hengyu 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2009年第8期1028-1035,共8页
Although considerable research has been conducted on nitrate reduction by zero-valent iron powder (Fe^0), these studies were mostly operated under anaerobic conditions with invariable pH that was unsuitable for prac... Although considerable research has been conducted on nitrate reduction by zero-valent iron powder (Fe^0), these studies were mostly operated under anaerobic conditions with invariable pH that was unsuitable for practical application. Without reaction conditions (dissolved oxygen or reaction pH) control, this work aimed at subjecting the kinetics of denitrification by microscale Fe^0 (160-200 mesh) to analysis the factors affecting the denitrification of nitrate and the composition of iron reductive products coating upon the iron surface. Results of the kinetics study have indicated that a higher initial concentration of nitrate would yield a greater reaction rate constant. The reduction rate of nitrate increased with increasing Fe^0 dosage. The reaction can be described as a pseudo-first order reaction with respect to nitrate concentration or Fe^0 dosage. Experimental results also suggested that nitrate reduction by microscale Fe^0 without reaction condition control primarily was an acid-driven surface-mediated process, and the reaction order was 0.65 with respect to hydrogen ion concentration. The analyses of X-ray diffractometry and X-ray photoelectron spectroscopy indicated that a black coating, consisted of Fe2O3, Fe3O4 and FeO(OH), was formed on the surface of iron grains as an iron corrosion product when the system initial pH was lower than 5. The proportion of FeO(OH) increased as reaction time went on, whereas the proportion of Fe3O4 decreased. 展开更多
关键词 KINETICS nitrate reduction zero-valent iron corrosion products PH
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Reductive denitrification of nitrate by scrap iron filings 被引量:2
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作者 郝志伟 徐新华 汪大翚 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE EI CAS CSCD 2005年第3期182-186,共5页
Reduction of nitrate by zero-valent iron is a highly exergonic reaction that has long been known to occur. Use of scrap iron filings (SIF) as the PRB (Permeable Reactive Barrier) material can be used to recycle certai... Reduction of nitrate by zero-valent iron is a highly exergonic reaction that has long been known to occur. Use of scrap iron filings (SIF) as the PRB (Permeable Reactive Barrier) material can be used to recycle certain by-products, and identify cheaper replacements for expensive conventional PRB materials, especially pure metallic iron. The feasibility of reductive denitrification of nitrate by SIF was studied by batch experiments. Operational parameters such as pH value, SIF dosage and initial concentration of nitrate were investigated. The removal efficiency of nitrate reached 80% under the conditions of pH of 2.5, nitrate initial con- centration of 45 mg/L and SIF dosage of 100 g/L within 4 h. Results indicated that nitrate removal is inversely related to pH. Low pH value condition favors for the nitrate transformation. Different from the results of others who studied nitrate reduction using iron powder, we found that there was a lag time before nitrate reduction occurs, even at low pH. Finally, the possible mechanism of nitrate reduction by Fe0 is discussed. 展开更多
关键词 DENITRIFICATION Scrap iron filings (SIF) Zero-valent iron nitrate MECHANISM
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Science Letters:Simultaneous removal of nitrate and heavy metals by iron metal 被引量:1
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作者 郝志伟 徐新华 +3 位作者 金剑 何平 刘永 汪大翚 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2005年第5期307-310,共4页
Great attention should be paid now to simultaneously removing common pollutants, especially inorganic pollutants such as nitrate and heavy metals, as individual removal has been investigated extensively. Removing comm... Great attention should be paid now to simultaneously removing common pollutants, especially inorganic pollutants such as nitrate and heavy metals, as individual removal has been investigated extensively. Removing common pollutants simul- taneously by iron metal is a very effective alternative method. Near neutral pH, heavy metals, such as copper and nickel, can be removed rapidly by iron metal, while nitrate removal very much slower than that of copper and nickel, and copper can accelerate nitrate removal when both are removed simultaneously. Even a little amount of copper can enhance nitrate removal efficiently. Different mechanisms of these contaminants removal by iron metal were also discussed. 展开更多
关键词 Simultaneously removing iron metal nitrate Heavy metal
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Synthesis of nanoscale zero-valent iron supported on exfoliated graphite for removal of nitrate 被引量:10
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作者 张环 金朝晖 +1 位作者 韩璐 秦承华 《中国有色金属学会会刊:英文版》 CSCD 2006年第B01期345-349,共5页
Nano ZVI particles supported on micro-scale exfoliated graphite were prepared by using KBH4 as reducing agent in the H2O/ethanol system. The supported ZVI materials generally have higher activity and greater flexibili... Nano ZVI particles supported on micro-scale exfoliated graphite were prepared by using KBH4 as reducing agent in the H2O/ethanol system. The supported ZVI materials generally have higher activity and greater flexibility for environmental remediation applications. The exfoliated graphite as the support was treated beforehand to hydrophilic material. Nano iron particles are deposited onto the rough graphite surface while those were formed by borohydride reduction. The possible nitrate reduction pathways were proposed. The TEM image shows that iron particles are highly dispersed on the surface of graphite and several of iron particles are imbedded in the pit of support surface. In this synthesis, iron particles have a nearly spherical shape with a grain size of 50?100 nm. The surface areas of materials with different iron loadings of 3.5%, 7.0%, 10.0%, 15.0% and 20.0%(mass fraction) are 2.89, 9.55, 8.45, 23.8 and 6.18 m2·g?1 by BET surface analyzer. The chemical reduction of nitrate by supported nano ZVI in aqueous solution were tested in series batch experiments. Experiment results suggest that NO3? can be more rapidly reduced to NH4+ at neutral pH and anaerobic conditions by supported nano ZVI than unsupported nano ZVI or ZVI scraps. The 15% nano Fe/graphite shows the best reduction efficiency contrasted with other Fe loading particles. 展开更多
关键词 纳米级0价铁粒子 合成 片状剥落石墨 载体 硝酸盐脱除
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不同Mn/Fe比例天然含铁锰矿的As(Ⅲ)吸附性能与机制
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作者 田周炀 郑倩 +3 位作者 杜晓丽 陈成 李传维 涂书新 《环境化学》 CAS CSCD 北大核心 2024年第8期2717-2727,共11页
水体中的砷主要以亚砷酸(As(Ⅲ))形态存在.金属氧化物常用于水体砷的去除,但其对As(Ⅲ)的亲和力较弱,导致水体砷很难去除,因此,寻求高效、廉价、绿色的除As(Ⅲ)材料具有显著的环境意义.天然含铁锰矿是一种高效的砷吸附剂,由于自然形成... 水体中的砷主要以亚砷酸(As(Ⅲ))形态存在.金属氧化物常用于水体砷的去除,但其对As(Ⅲ)的亲和力较弱,导致水体砷很难去除,因此,寻求高效、廉价、绿色的除As(Ⅲ)材料具有显著的环境意义.天然含铁锰矿是一种高效的砷吸附剂,由于自然形成条件复杂,其不同含铁锰矿对As(Ⅲ)的去除性能存在较大差异.本研究以两种不同Mn/Fe比例的天然含铁锰矿(NFM-L、NFM-H)为研究对象,评估其对As(Ⅲ)的吸附性能,并结合XPS、XRD等光谱学表征手段探究其砷的去除机制.实验结果表明,NFM-L的Fe含量是NFM-H的5.61倍,其As(Ⅲ)的最大吸附量(24.82 mg·g^(−1))与吸附速率亦显著高于NFM-H(18.94 mg·g^(−1)),NFM-L和NFM-H对As(Ⅲ)的等温吸附曲线更符合Freundlich模型.影响因子实验表明,溶液pH值对NFM-L的影响更大,共存离子H_(2)PO_(4)^(−)能够显著抑制两种材料对As(Ⅲ)的吸附,但是材料粒径对As(Ⅲ)去除的影响较小.光谱学表征发现,两种矿物吸附砷后结构并未发生明显变化,但锰氧化物能将As(Ⅲ)氧化为As(V),从而显著提高了铁锰矿对砷的吸附能力. 展开更多
关键词 天然含铁锰矿 As() Mn/Fe 氧化 吸附.
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Nitrogen removal efficiency of iron-carbon micro-electrolysis system treating high nitrate nitrogen organic pharmaceutical wastewater 被引量:4
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作者 周健 段送华 +1 位作者 陈垚 胡斌 《Journal of Central South University》 SCIE EI CAS 2009年第S1期368-373,共6页
The nitrate nitrogen removal efficiency of iron-carbon micro-electrolysis system was discussed in treating pharmaceutical wastewater with high nitrogen and refractory organic concentration. The results show that the g... The nitrate nitrogen removal efficiency of iron-carbon micro-electrolysis system was discussed in treating pharmaceutical wastewater with high nitrogen and refractory organic concentration. The results show that the granularity of fillings,pH,volume ratios of iron-carbon and gas-water,and HRT. have significant effects on the nitrogen removal efficiency of iron-carbon micro-electrolysis system. The iron-carbon micro-electrolysis system has a good removal efficiency of pharmaceutical wastewater with high nitrogen and refractory organic concentration when the influent TN,NH4+-N,NO3--N and BOD5/CODCr are 823 mg/L,30 mg/L,793 mg/L and 0.1,respectively,at the granularity of iron and carbon 0.425 mm,pH 3,iron-carbon ratio 3,gas-water ratio 5,HRT 1.5 h,and the removal rates of TN,NH4+-N and NO3--N achieve 51.5%,70% and 50.94%,respectively. 展开更多
关键词 iron-CARBON MICRO-ELECTROLYSIS NITROGEN nitrate NITROGEN REMOVAL efficiency REMOVAL rate
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综合化学实验设计:氧桥三核铁(Ⅲ)配合物的便捷制备与表征
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作者 楚进锋 王艺澄 +5 位作者 齐继 刘余霖 李言 靳兰 何蕾 宋宇飞 《大学化学》 CAS 2024年第7期299-306,共8页
目前本科化学实验教学内容在配合物制备实验方面主要涵盖了单核配合物,而对配合物家族中占有重要地位的多核配合物却很少涉及。基于此,我们依据科研成果设计了一个关于三核铁(Ⅲ)配合物的综合化学实验,以期通过该实验加深学生对配合物... 目前本科化学实验教学内容在配合物制备实验方面主要涵盖了单核配合物,而对配合物家族中占有重要地位的多核配合物却很少涉及。基于此,我们依据科研成果设计了一个关于三核铁(Ⅲ)配合物的综合化学实验,以期通过该实验加深学生对配合物有关知识的理解和运用。本设计以廉价易得的九水合硝酸铁与三水合乙酸钠为原料,通过水浴加热反应、冷却结晶等步骤制备了一种氧桥三核铁(Ⅲ)配合物[Fe_(3)O(CH_(3)COO)_(6)(H_(2)O)_(3)]NO_(3)·4H_(2)O,通过配位滴定法测定了其铁元素含量,并对其进行了红外、热重、粉末X射线衍射和电子顺磁共振等表征测试。该实验制备方法简单快捷,易于操作,环保无污染。实验内容蕴含思政元素,目标配合物结构新颖,富有对称美,实验教学时亦可培养学生的审美意识,使其领略化学之美。本设计科教融合,有助于培养学生分析解决问题的能力,为本科生的综合化学实验教学提供了一个可行案例。 展开更多
关键词 综合化学实验 氧桥三核铁()配合物 对称结构 电子顺磁共振
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Study on the Removal of Iron,Manganese and Nitrate in Groundwater by Biological Ribbon Technology
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作者 Yuchen Li,Yukun Ju School of Water Resources & Environment,China University of Geosciences(Beijing),Beijing 100083,China 《地学前缘》 EI CAS CSCD 北大核心 2009年第S1期190-191,共2页
The pollution of iron,manganese and nitrate in groundwater is a huge threat to human beings.In this study,column experiments of ceramic,manganese sand,ceramic sand,volcanic rock,quartz sand were conducted.Iron and man... The pollution of iron,manganese and nitrate in groundwater is a huge threat to human beings.In this study,column experiments of ceramic,manganese sand,ceramic sand,volcanic rock,quartz sand were conducted.Iron and manganese contents of influent were 3.3 mg/L and 2.1 mg/L.When the biofilm became mature,the highest iron and manganese removal rate achieved by manganese sand as a filter material.Quartz did a little worse than manganese sand,but other three filter material could not reach 展开更多
关键词 removal of iron MANGANESE and nitrate GROUNDWATER BIOLOGICAL RIBBON technology
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Preparation of Nanoiron by Water-in-Oil (W/O) Microemulsion for Reduction of Nitrate in Groundwater
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作者 Tielong LI Shujing LI +2 位作者 Shuaima WANG Yi AN Zhaohui JIN 《Journal of Water Resource and Protection》 2009年第1期16-21,共6页
Nanometer-sized iron particles with monodispersity and narrow size distribution were synthesized by modi-fied microemulsion system using environment-friendly non-ionic surfactants Span 80 and Tween 60 as mixed surfact... Nanometer-sized iron particles with monodispersity and narrow size distribution were synthesized by modi-fied microemulsion system using environment-friendly non-ionic surfactants Span 80 and Tween 60 as mixed surfactants. The synthesized iron nanoparticles were characterized by using powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results show that the synthesized particles were mainly composed of α-Fe with an average diameter of 80-90 nm. The chemical activity of the obtained iron nanoparticles was evaluated by the denitrification of nitrate in water. On neutral condition, complete denitri-fication of nitrate was achieved by freshly synthesized nanoiron within 30 min. Ammonia was the main product, with good material balance at the end of the reaction. Two possible reaction pathways for nitrate reduction by nanoiron have been proposed in this study. 展开更多
关键词 iron Nanoparticles MICROEMULSION REDUCTION nitrate
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Remediation of Nitrate and ChromiumContaminated Groundwater by Zero-valent IronPRB
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《环境科学前沿(中英文版)》 2015年第2期39-45,共7页
Through continuous flow experimentation, the reactivity characteristics of zero-valent iron (Fe0)-PRB with ground watercontaminated by nitrate, chromium and the combination of nitrate and chromium were investigated.... Through continuous flow experimentation, the reactivity characteristics of zero-valent iron (Fe0)-PRB with ground watercontaminated by nitrate, chromium and the combination of nitrate and chromium were investigated. The results showed thatnitrate could be effectively deoxidized by zero-valent iron. NO^2- -N was the transitional deoxidization product, while NH4+-Nwas the main final product in the effluent. Chromium could be deoxidized by zero-valent iron more effectively for the chromiumcontaminated ground water which was treated by PRB. The redox products such as Fe3+ and Cr(III) precipitated on the packingmedia during the process. For the treatment of ground water contaminated by both nitrate and chromium, the results showed thatthe Cr(VI) removal efficiency by the zero-valent iron was not affected by the co-existence of NO^3- -N, while the NO^3- -N removalefficiency decreased with the existence of Cr(VI). 展开更多
关键词 Zero-valent iron PERMEABLE Reactive Barrier(PRB) Ground Water nitrate CHROMIUM
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Photochemical degradation of environmentally persistent perfluorooctanoic acid (PFOA) in the presence of Fe(Ⅲ) 被引量:3
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作者 Yuan Wang Peng Yi Zhang +1 位作者 Gang pan Hao chen 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第3期371-374,共4页
Environmentally persistent and bioaccumulative perfluorooctanic acid (PFOA) was difficult to be decomposed under the irradiation of 254 nm UV light. However, in the presence of 80μmol/L Fe(Ⅲ), 80% of PFOA with i... Environmentally persistent and bioaccumulative perfluorooctanic acid (PFOA) was difficult to be decomposed under the irradiation of 254 nm UV light. However, in the presence of 80μmol/L Fe(Ⅲ), 80% of PFOA with initial concentration of 48μmol/L (20 mg/L) was effectively degraded and 47.8% of fluorine atoms in PFOA molecule were transformed into inorganic fluoride ion after 4 h reaction. Shorter chain perfluorocarboxylic acids bearing C3-C7 and fluoride ion were detected and identified by LC/MS and IC as the degradation products in the aqueous solution. It was proposed that complexes of PFOA with Fe(Ⅲ) initiated degradation of PFOA irradiated with 254 nm UV light. 展开更多
关键词 Perfluorooctanoic acid iron( Photochemical degradation 254 nm UV light
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炭化与焙烧温度对植物基铁碳微电解材料去除As(Ⅲ)性能的影响 被引量:1
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作者 李海东 杨远坤 +7 位作者 郭姝姝 汪本金 岳婷婷 傅开彬 王哲 何守琴 姚俊 谌书 《化工进展》 EI CAS CSCD 北大核心 2023年第7期3652-3663,共12页
以美人蕉、还原铁粉和膨润土为原材料制备植物基铁碳微电解材料,先通过单因素实验确定Fe/C物质的量比、炭化温度和焙烧温度3个影响因素,后采用Box-Behnken响应面法对“均质化-炭化-焙烧”制备工艺进行优化,以确定最优制备条件。并结合X... 以美人蕉、还原铁粉和膨润土为原材料制备植物基铁碳微电解材料,先通过单因素实验确定Fe/C物质的量比、炭化温度和焙烧温度3个影响因素,后采用Box-Behnken响应面法对“均质化-炭化-焙烧”制备工艺进行优化,以确定最优制备条件。并结合X射线衍射(XRD)、电子顺磁共振波谱仪(EPR)、傅里叶红外光谱仪(FTIR)等表征方法,探究烧制温度对植物基铁碳微电解材料固有性质及其去除As(Ⅲ)性能的影响。结果表明,最优制备条件为Fe/C=1.05、炭化温度502.87℃、焙烧温度760.92℃。烧制温度的升高,有利于增强碳基组分得电子能力,加速As(Ⅲ)氧化为As(Ⅴ),降低水体生物毒性的同时提高对As(Ⅲ)的去除率;当焙烧温度高于700℃时,膨润土晶体结构层瓦解,渗透性提高的同时加速Ca^(2+)、Mg^(2+)离子释放,并促进Fe^(3+)的水解沉积物互斥作用减弱,提高对As(Ⅲ)的吸附容量;还原铁粉过量5%,在保证反应时微原电池数量的同时,表面氧化产生的Fe_(3)O_(4)、Fe_(2)O_(3)在酸性条件下易反应形成Fe^(2+)、Fe^(3+),对As(Ⅲ)的吸附去除作用加强。 展开更多
关键词 铁碳微电解材料 As() 响应面优化 热解 电化学 造粒
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Simple, Selective, and Sensitive Spectrophotometric Method for Determination of Trace Amounts of Nickel(Ⅱ), Copper (Ⅱ), Cobalt (Ⅱ), and Iron (Ⅲ) with a Novel Reagent 2-Pyridine Carboxaldehyde Isonicotinyl Hydrazone 被引量:2
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作者 Sajid H. Guzar JIN Qin-han 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2008年第2期143-147,共5页
A selective and sensitive reagent of 2-pyridine carboxaldehyde isonicotinyl hydrazone(2-PYAINH) was synthesized and studied for the spectrophotometric determination of nickel, copper, cobalt, and iron in detail. At ... A selective and sensitive reagent of 2-pyridine carboxaldehyde isonicotinyl hydrazone(2-PYAINH) was synthesized and studied for the spectrophotometric determination of nickel, copper, cobalt, and iron in detail. At a pH value of 7.0, 9,0, 9.0, and 8.0, respectively, which greatly increased the selectivity; nickel, copper, cobalt, and iron reacted with 2-PYAINH to form a 1:2 yellow-orange, 1:2 yellow-green, 1:2 yellow and 1:1 yellow complexes, with absorption peaks at 363, 352, 346, and 359 nm, respectively. Under the optimal conditions, Beer's law was obeyed over the ranges of 0.01-1.4, 0.01-1.5, 0.01-2.7, and 0.01-5.4 mg/L respectively. The apparent molar absorptivity and Sandell's sensitivities were 8.4×10^4, 5.2×10^4, 7.1×10^4, and 3.9×10^4 L·mol^-l·cm^-1, respectively, and 0.00069, 0.0012, 0.00078, and 0.0014 μg·cm2, respectively. The detection limits were found to be 0.001, 0.002, 0.003, and 0.01 mg/L, respectively. The detailed study of various interfering ions to make the method more sensitive was carried out and selective and several real samples were analyzed with satisfactory results. 展开更多
关键词 Copper(Ⅱ) Nickel(Ⅱ) Cobalt(Ⅱ) iron( 2-Pyridine carboxaldehyde isonicotinyl hydrazone(2-PYAINH) SPECTROPHOTOMETRY
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Characterization of Aquabacterium parvum sp. Strain B6 during Nitrate-Dependent Fe(Ⅱ) Oxidation Batch Cultivation with Various Impact Factors 被引量:2
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作者 Xiaoxin Zhang Ulrich Szewzyk Fang Ma 《Transactions of Tianjin University》 EI CAS 2017年第4期315-324,共10页
In order to assess the capacity of Aquabacterium parvum sp. strain B6 for nitrate-dependent Fe(II) oxidation, batch cultivation was conducted, and its ability to oxidize Fe(II) coupled to nitrate reduction in the pres... In order to assess the capacity of Aquabacterium parvum sp. strain B6 for nitrate-dependent Fe(II) oxidation, batch cultivation was conducted, and its ability to oxidize Fe(II) coupled to nitrate reduction in the presence of diverse organic substrates was studied. Meanwhile, the nitrate-removal rate of B6 with various impact factors was further optimized by the response surface methodology (RSM). The results show that strain B6 is capable of utilizing different organic compounds as substrates for nitrate reduction. Compared with yeast extract, B6 showed a greater potential of chemical oxygen demand (COD) degradation and cell proliferation with acetate and glucose mediums, respectively, while citrate was not beneficial for this process due to its low consumption rate. RSM analysis demonstrated that the maximum nitrate-reduction rate of 30.64% could be achieved with an initial pH of 7.4, incubation temperature of 25.0 °C, and carbon source concentration of 266.10 mg/L. © 2017, Tianjin University and Springer-Verlag Berlin Heidelberg. 展开更多
关键词 Carbon Cell proliferation iron compounds nitrateS Optimization OXIDATION
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铜离子选择性电极研究铁(Ⅲ)与Tiron,HOx配位化合物
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作者 魏昌明 陈连山 +1 位作者 马桂芝 何钟林 《辽宁师范大学学报(自然科学版)》 CAS 1994年第3期217-221,共5页
用固态膜铜离子选择性电极研究Fe(Ⅲ)与1,2-二羟基苯-3,5-二磺酸钠溶液配合物的组成和表观稳定常数.离于强度I=0.1mol·L-1,pH=2.1时生成1:1型配合物,pH=3.08时Fe(Ⅲ)与8-羟基喹... 用固态膜铜离子选择性电极研究Fe(Ⅲ)与1,2-二羟基苯-3,5-二磺酸钠溶液配合物的组成和表观稳定常数.离于强度I=0.1mol·L-1,pH=2.1时生成1:1型配合物,pH=3.08时Fe(Ⅲ)与8-羟基喹啉生成1:1和1:2型两种溶液配位化合物. 展开更多
关键词 铁络合物 离子选择电极
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Electric Conductivity Study of o-Substituted Phenoxo Iron (Ⅲ) Complexes 被引量:2
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作者 Ramadan Ali Bawa 《Journal of Chemistry and Chemical Engineering》 2010年第5期54-58,共5页
The coordination nature of a number of substituted sodiumphenoxides to iron (Ⅲ) ion has been studied. The o-nitrosodiumphenoxide was found to have different coordination behaviour from that the sodium salts of sali... The coordination nature of a number of substituted sodiumphenoxides to iron (Ⅲ) ion has been studied. The o-nitrosodiumphenoxide was found to have different coordination behaviour from that the sodium salts of salicylic acid and methylsalicylate showed. The structure of the complexes, the number of the ligands being coordinated to the metal ion, has also been determined by titration, uv-vis spectroscopy, atomic absorption and the flame test. In addition, other sodium phenoxides were also involved in this study for comparison. An electric conductivity study on the resulting complexes was carried out and all complexes were found to be semiconductors. 展开更多
关键词 iron ion COMPLEXES COORDINATION electric conductivity SEMICONDUCTORS
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磷石膏基复合吸附材料的制备及其对废水中As(Ⅲ)的吸附性能研究 被引量:3
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作者 吕晨阳 许向群 +2 位作者 宋云杰 马梦雨 杜亚光 《湿法冶金》 CAS 北大核心 2023年第2期163-171,共9页
研究了用机械球磨法混合磷石膏(PG)和还原铁粉制备吸附材料(m-PG-Fe),通过响应面法对制备工艺条件进行优化,考察了优化条件下所制备m-PG-Fe对模拟废水中As(Ⅲ)的吸附性能。结果表明:最优制备条件为PG配比60%,球磨转速500 r/min,球磨时间... 研究了用机械球磨法混合磷石膏(PG)和还原铁粉制备吸附材料(m-PG-Fe),通过响应面法对制备工艺条件进行优化,考察了优化条件下所制备m-PG-Fe对模拟废水中As(Ⅲ)的吸附性能。结果表明:最优制备条件为PG配比60%,球磨转速500 r/min,球磨时间为2 h;在该条件下制备的m-PG-Fe对废水中As(Ⅲ)的吸附量为29.86 mg/g,与预测值的误差为3.7%,可靠性较高,具有潜在使用价值;m-PG-Fe具有更大的比表面积、孔隙体积和介孔率,在机械力作用下PG中的结晶水逸出产生羟基自由基,并与铁粉在球磨作用下结合生成FeO(OH),有利于对As(Ⅲ)的吸附。 展开更多
关键词 磷石膏 铁粉 球磨 响应面法 吸附 As()
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土壤铁锰氧化物形态测定及吸附Sb(Ⅲ)的主控因子研究 被引量:4
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作者 崔婷 叶欣 +2 位作者 朱霞萍 李军亚 徐欢 《岩矿测试》 CAS CSCD 北大核心 2023年第1期167-176,共10页
研究影响土壤吸附Sb(Ⅲ)的主控因子对土壤锑污染的评价、预警及修复具有重要意义。本文采用化学法、电感耦合等离子体发射光谱法和原子荧光光谱法测定了10个不同地区土壤的理化性质和机械组成、主要化学组成,采用原子吸收光谱法测定了... 研究影响土壤吸附Sb(Ⅲ)的主控因子对土壤锑污染的评价、预警及修复具有重要意义。本文采用化学法、电感耦合等离子体发射光谱法和原子荧光光谱法测定了10个不同地区土壤的理化性质和机械组成、主要化学组成,采用原子吸收光谱法测定了土壤铁锰氧化物的不同形态以及土壤对Sb(Ⅲ)的饱和吸附容量,并开展了土壤对Sb(Ⅲ)的饱和吸附容量和土壤理化性质、机械组成、铁锰氧化物及其形态的相关性分析、主成分分析和因子分析。在研究土壤吸附Sb(Ⅲ)的影响因素基础上,进一步研究其主控因子。结果表明,10个不同性质的土壤对Sb(Ⅲ)饱和吸附容量介于0.63~3.98mg/g之间,与土壤类型有关,其大小顺序为:红壤>棕壤>黄壤>褐土>沙土。土壤对Sb(Ⅲ)饱和吸附容量与阳离子交换容量(CEC)、氧化铁总量、无定形铁含量呈极显著正相关,与游离铁含量、无定形锰含量以及游离锰含量呈显著正相关。主成分分析和因子分析结果表明土壤中6个因子是影响土壤吸附Sb(Ⅲ)的主控因子,影响力大小为:氧化铁总量>CEC>无定形铁含量>游离铁含量>无定形锰含量>游离锰含量。铁锰氧化物及其形态显著影响土壤吸附Sb(Ⅲ)。 展开更多
关键词 土壤 Sb() 吸附 主控因子 铁锰氧化物形态 原子吸收光谱法
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酸溶液中溶剂萃取法分离钼(Ⅵ)/铁(Ⅲ)的研究进展 被引量:2
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作者 李飞 彭苗苗 +4 位作者 胡智怡 刘纯 肖莉琼 刘志雄 颜文斌 《矿冶工程》 CAS 北大核心 2023年第2期118-124,129,共8页
分析了不同溶液酸度条件下钼、铁离子的存在形态,并依此对现有的钼/铁溶剂萃取分离方法进行了分类,讨论了各方法的原理、效果及其优缺点。并对未来溶剂萃取法钼/铁分离可能的发展方向进行了展望,以期能为绿色、高效的酸溶液中钼/铁萃取... 分析了不同溶液酸度条件下钼、铁离子的存在形态,并依此对现有的钼/铁溶剂萃取分离方法进行了分类,讨论了各方法的原理、效果及其优缺点。并对未来溶剂萃取法钼/铁分离可能的发展方向进行了展望,以期能为绿色、高效的酸溶液中钼/铁萃取分离新工艺研发及应用提供思路。 展开更多
关键词 酸法提钼 溶剂萃取 钼/铁分离 离子液体 抑制效应 Mo(Ⅵ) Fe()
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Chemical reduction of nitrate by nanoscale Fe/Ni bimetallic particles 被引量:1
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作者 Haiyan KANG Zongming XIU Lili SUN Tielong LI Zhenying LIU Zhaohui JIN 《Chinese Journal Of Geochemistry》 EI CAS 2006年第B08期111-112,共2页
关键词 二金属颗粒 反硝化作用 硝酸盐 地下水 水体污染
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