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13C交叉极化魔角旋转核磁共振光谱法作为一种通用的定量工具,用于测定硫醇功能化介孔二氧化硅SBA-1中的汞吸附容量。

13C CPMAS NMR spectroscopy as a versatile and quantitative tool for determination of mercury adsorption capacity in thiol-functionalized mesoporous silica SBA-1.

作者信息

Kao Hsien-Ming, Lee Lung-Ping, Palani Arudra

机构信息

Department of Chemistry, National Central University, Chung-Li, Taiwan 32054, ROC.

出版信息

Anal Chem. 2008 Apr 15;80(8):3016-9. doi: 10.1021/ac702356h. Epub 2008 Mar 14.

Abstract

13C cross-polarization magic angle spinning (CPMAS) NMR spectroscopy is demonstrated to be a valuable characterization tool for quantitative measurements of Hg2+ adsorption capacity in thiol-functionalized mesoporous silica SBA-1 (Santa Barbara Amorphous-1). This is the first report on the investigation of the spectral change in the 13C CP signals for mercaptopropyl-functionalized mesoporous materials doped with different Hg2+ concentrations. The chemical shift of the carbon atom adjacent to the thiol group is sensitive to the binding of the mercury ion, and its peak intensity can be used as a quantitative sensor for the amount of the mercury ion adsorbed. The 13C CPMAS NMR results are in good agreement with inductively coupled plasma-atomic emission spectroscopy (ICP-AES) analysis.

摘要

13C交叉极化魔角旋转(CPMAS)核磁共振光谱被证明是一种用于定量测量硫醇功能化介孔二氧化硅SBA - 1(圣巴巴拉无定形 - 1)中Hg2+吸附容量的有价值的表征工具。这是关于研究不同Hg2+浓度掺杂的巯基丙基功能化介孔材料的13C CP信号光谱变化的首次报告。与硫醇基团相邻的碳原子的化学位移对汞离子的结合很敏感,其峰强度可作为吸附汞离子量的定量传感器。13C CPMAS NMR结果与电感耦合等离子体原子发射光谱(ICP - AES)分析结果吻合良好。

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