Suppr超能文献

水溶液中氯化钾的分子动力学和中子散射研究。

Molecular Dynamics and Neutron Scattering Studies of Potassium Chloride in Aqueous Solution.

机构信息

Institute of Organic Chemistry and Biochemistry , Academy of Sciences of the Czech Republic & Center for Biomolecules and Complex Molecular Systems , 16610 Prague 6 , Czech Republic.

Department of Food Science , Cornell University , Ithaca , New York 14853 , United States.

出版信息

J Phys Chem B. 2019 Dec 19;123(50):10807-10813. doi: 10.1021/acs.jpcb.9b08422. Epub 2019 Dec 10.

Abstract

Neutron diffraction with isotopic substitution (NDIS) experiments were done on both natural abundance potassium and isotopically labeled KCl heavy water solutions to characterize the solvent structuring around the potassium ion in water. Preliminary measurements suggested that the literature value for the coherent neutron scattering length (2.69 fm) for K was significantly in error. This value was remeasured using a neutron powder diffractometer and found to be 2.40 fm. This revision increases significantly the contrast between the natural abundance K and K by about 30% (from 1.0 to 1.3 fm). The experimentally determined structure factor of the potassium ion was then compared to that calculated from molecular dynamics (MD) simulations. Previous neutron scattering measurements of potassium gave a solvation number of 5.5 (see below). In this study, the NDIS and MD results are in good agreement and allowed us to derive a coordination number of 6.1 for water molecules and 0.8 for chloride ions around each K ion in 4 molal aqueous KCl solution.

摘要

利用同位素取代的中子衍射(NDIS)实验对天然丰度的钾和同位素标记的 KCl 重水溶液进行了研究,以表征水中钾离子周围的溶剂结构。初步测量表明,文献中钾的相干中子散射长度(2.69 fm)值存在显著误差。使用中子粉末衍射仪重新测量了该值,发现为 2.40 fm。这一修正显著增加了天然丰度 K 和 K 之间的对比度约 30%(从 1.0 到 1.3 fm)。然后将实验测定的钾离子结构因子与分子动力学(MD)模拟计算的结构因子进行了比较。先前的钾中子散射测量得到的溶剂化数为 5.5(见下文)。在这项研究中,NDIS 和 MD 的结果非常吻合,使我们能够得出在 4 molal 的 KCl 水溶液中,每个 K 离子周围的水分子配位数为 6.1,氯离子配位数为 0.8。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验