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利用液相脉冲激光烧蚀制备的铁@石墨/钯(Fe@C/Pd)纳米颗粒强化间二氯苯的脱氯作用。

Enhanced dechlorination of m-DCB using iron@graphite/palladium (Fe@C/Pd) nanoparticles produced by pulsed laser ablation in liquid.

作者信息

Yu Yiseul, Jung Hyeon Jin, Je Mingyu, Choi Hyun Chul, Choi Myong Yong

机构信息

Department of Chemistry (BK21 PLUS) and Research Institute of Natural Science, Gyeongsang National University, Jinju, 660-701, Republic of Korea.

Department of Chemistry, Chonnam National University, Gwangju, 500-757, Republic of Korea.

出版信息

Chemosphere. 2016 Jul;155:250-256. doi: 10.1016/j.chemosphere.2016.04.048. Epub 2016 Apr 26.

Abstract

In this work, the zero valent Fe (ZVI) and graphite-encapsulated Fe (Fe@C) nanoparticles (NPs) were easily and selectively prepared by a pulsed laser ablation (PLA) method in an aqueous sodium borohydride solution and ascorbic acid dissolved in methanol, respectively. Here, the Fe@C NPs were uniquely synthesized by PLA in methanol, where the solvent is used as both a carbon source for the graphitic layers and solvent, which is very unique. Furthermore, Pd NPs were loaded onto the surface of the Fe@C NPs to prepare bimetallic (Fe@C/Pd) NPs for the enhancement of the degradation efficiency of m-dichlorobenzene (m-DCB). The morphology, crystallinity, and surface composition of the prepared NPs were carefully characterized by high-resolution transmission electron microscopy (HRTEM), energy dispersive x-ray spectrometer (EDS), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The degradation rate of m-DCB using single (Fe and Pd) or bimetallic (Fe/Pd and Fe@C/Pd) NPs were compared by using gas chromatography. Among these NPs produced in this work, the Fe@C/Pd NPs with 1.71 wt % of Pd showed an excellent dechlorination efficiency for m-DCB with 100% degradation within 75 min. The graphitic layer on the Fe NPs played as not only an oxidation resistant for the Fe NPs to surroundings, but also a supporter of the Pd NPs for the enhanced degradation efficiency of m-DCB.

摘要

在本工作中,分别通过脉冲激光烧蚀(PLA)法在硼氢化钠水溶液和溶解于甲醇的抗坏血酸中,轻松且选择性地制备了零价铁(ZVI)和石墨包覆铁(Fe@C)纳米颗粒(NPs)。在此,Fe@C NPs是通过PLA在甲醇中独特合成的,其中溶剂既用作石墨层的碳源又用作溶剂,这非常独特。此外,将钯纳米颗粒负载到Fe@C NPs表面,制备双金属(Fe@C/Pd)纳米颗粒,以提高间二氯苯(m-DCB)的降解效率。通过高分辨率透射电子显微镜(HRTEM)、能量色散X射线光谱仪(EDS)、X射线衍射(XRD)和X射线光电子能谱(XPS)仔细表征了所制备纳米颗粒的形态、结晶度和表面组成。使用气相色谱法比较了使用单金属(Fe和Pd)或双金属(Fe/Pd和Fe@C/Pd)纳米颗粒时m-DCB的降解率。在本工作制备的这些纳米颗粒中,含1.71 wt% Pd的Fe@C/Pd纳米颗粒对m-DCB表现出优异的脱氯效率,在75分钟内降解率达100%。铁纳米颗粒上的石墨层不仅对铁纳米颗粒起到抗周围环境氧化的作用,而且作为钯纳米颗粒的载体提高了m-DCB的降解效率。

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