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Characterization of nZVI nanoparticles functionalized by EDTA and dipicolinic acid: a comparative study of metal ion removal from aqueous solutions

机译:EDTA和二吡啶甲酸功能化的nZVI纳米颗粒的表征:水溶液中金属离子去除的比较研究

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The simultaneous adsorption of metal ions on bare and functionalized zero-valent iron nanoparticles (nZVI) from aqueous solution was tested using inductively coupled plasma optical emission spectrometry (ICP-OES). The nanomaterials were synthetized using borohydride reduction of iron salt followed by addition of EDTA and pyridine-2,6-dicarboxylic acid (dipicolinic acid, PDCA) in different molar ratios. Functionalized materials were characterized by FT-IR, XRD and SEM-EDS methods. The ligand attachment on the particles was confirmed by FT-IR spectroscopy. The formation of a magnetite and feroxyhyte shell on the core of functionalized nanoparticles was confirmed by the XRD study. Transformation of chain-like structures into clusters of nanospheres with smaller diameter size was observed from SEM study of EDTA-nVZI particles. The average diameter of bare nZVI particles comprised 115 nm, while EDTA functionalization resulted in an average diameter of 22 and 35 nm. The PDCA-nZVI particles obtained with the molar ratio of Fe?:?PDCA = 1?:?1 retain the chain-like structure with enlargement of the average particle diameter to 267 nm. SEM study of PDCA-nZVI particles that were produced using the ratio Fe?:?PDCA = 2?:?1 have demonstrated the unique property of elongation into ellipsoidal forms of reduced dimensions ( a = 61 nm; b = 28 nm). The simultaneous metal ion removal from aqueous solution was the most efficient in the case of bare nZVI particles (91–97%). EDTA functionalization was found to be highly selective for Cu and Cr removal (95%), while PDCA functionalization shows selective adsorption of Cu, Cr and V in an aqueous medium (93%). Iron nanoparticles functionalized with PDCA in both of the used ratios showed more efficient metal ion adsorption in the case when smaller ellipsoidal particles were formed.
机译:使用电感耦合等离子体发射光谱法(ICP-OES)测试了金属离子从水溶液中同时吸附在裸露的功能化零价铁纳米颗粒(nZVI)上的情况。使用硼氢化物还原铁盐,然后以不同的摩尔比添加EDTA和吡啶2,6-二羧酸(二吡啶甲酸,PDCA)来合成纳米材料。通过FT-IR,XRD和SEM-EDS方法对功能材料进行了表征。通过FT-IR光谱确认了配体在颗粒上的附着。 XRD研究证实,在功能化纳米颗粒的核上形成了磁铁矿和亚铁酸盐壳。从EDTA-nVZI颗粒的SEM研究中观察到链状结构转变成直径较小的纳米球簇。裸露的nZVI颗粒的平均直径为115 nm,而EDTA官能化的平均直径为22和35 nm。 Fe 2 ∶PDCA = 1∶1的摩尔比得到的PDCA-nZVI颗粒保持链状结构,平均粒径扩大到267nm。用Fe 2 ∶PDCA = 2 2 ∶β 1的比例生产的PDCA-nZVI颗粒的SEM研究表明,伸长成具有减小尺寸的椭圆形(a = 61nm; b = 28nm)的独特性质。对于裸露的nZVI粒子(91–97%),从水溶液中同时去除金属离子是最有效的。发现EDTA官能化对去除Cu和Cr具有很高的选择性(95%),而PDCA官能化对水介质中的Cu,Cr和V有选择性吸附(93%)。在两个较小的比例下,用PDCA官能化的铁纳米颗粒在形成较小的椭圆形颗粒时显示出更有效的金属离子吸附。

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