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Titlebook: Magnetic Resonance in Colloid and Interface Science; Jacques Fraissard,Olga Lapina Book 2002 Kluwer Academic Publishers 2002 Epoxidharze.H

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发表于 2025-3-21 16:13:25 | 显示全部楼层 |阅读模式
书目名称Magnetic Resonance in Colloid and Interface Science
编辑Jacques Fraissard,Olga Lapina
视频video
丛书名称NATO Science Series II: Mathematics, Physics and Chemistry
图书封面Titlebook: Magnetic Resonance in Colloid and Interface Science;  Jacques Fraissard,Olga Lapina Book 2002 Kluwer Academic Publishers 2002 Epoxidharze.H
描述.Magnetic resonance techniques are especially interesting in the study of colloids and interfaces due to their unique ability to elucidate structure, dynamics and function at the atomic and molecular level. This book illustrates the most up to date applications of innovative NMR and EPR techniques, including magnetic resonance imaging and microscopy, to gas-solid and liquid-solid interfaces, organic and biological surfaces, microemulsions, liquid crystals, membranes, structure and dynamics of polymers and micellar systems, and diffusion in heterogeneous systems. ..A compendium of advanced NMR and EPR techniques and a state of the art description of the power of advanced new methodologies for the study of molecular dynamics and interfaces. .
出版日期Book 2002
关键词Epoxidharze; Helium-Atom-Streuung; Nafion; Phenoplaste; Resol; Styrol-Butadien; adsorption; colloid; interfa
版次1
doihttps://doi.org/10.1007/978-94-010-0534-0
isbn_softcover978-1-4020-0787-3
isbn_ebook978-94-010-0534-0Series ISSN 1568-2609
issn_series 1568-2609
copyrightKluwer Academic Publishers 2002
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Quantifying Structural and Dynamic Disorder in Ionically Conducting Solid Solutionsent substitution of the mobile ions can greatly affect the magnitude of the electrical conductivity and the mechanism of ion transport in such materials, as a consequence of the spatial arrangement and ordering of the mobile ions involved. Solid State NMR techniques are uniquely suitable to address
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14N MAS NMR Spectroscopy. An Instrumental Challenge and Informatory Techniques are NMR active: .N (. = 1) and .N (.= 1/2) with abundances of 99.63% and 0.37%, respectively. Due to the unfavorable properties of the .N isotope it has rarely been targeted for NMR observation because it is considered a low-frequency nucleus of low sensitivity and because of the quadrupolar broad
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NMR Diffusion Studies of Molecules in Nanoporous Materialstensity pulsed magnetic field gradients in high-field sc magnets and of operation routines for an automated matching of such pulsed gradients, gave rise to a number of diffusion studies with porous materials, where new features of interrelation between host structure and guest mobility were observed
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NMR Studies of the Mesomorphism, Structure and Dynamics of Some New Pyramidic Liquid Crystalscores consist of flat medium size aromatic moieties, such as benzene, naphthalene and triphenylene, but more recently discogens with much larger cores, such as hexabenzocoronene have also been prepared [2, 3]. The side chains are usually normal aliphatic groups, which are linked to the core by ether
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“Lighting Up” NMR and MRI in Colloidal and Interfacial Systems polarization has allowed an extension of the pioneering experiments of Fraissard and coworkers to novel applications of NMR and MRI in chemistry, materials science and biomedicine. Examples are presented of developments and applications of laser-polarized xenon NMR and MRI on distance scales from n
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Progress in High Resolution Solid State NMR of Quadrupolar Nuclei: Applications to Porous Materials upling via REDOR. The advantage of these techniques is that they provide direct inference of the connectivities between spin- 1/2 and half-integer quadrupolar nuclei in the isotropic spectra of the latter. Additionally, the MQ- REDOR methods yield the internuclear distances in these systems. We have
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Applications of Hyperpolarized 129Xe NMR Spectroscopy to the Study of Materialsn idea is that the chemical shift tensor of Xe nuclides is extremely sensitive to local surroundings, primarily because of the large number of polarizable electrons [4, 5]. For small pore systems this is best summarized by stating that the isotropic shift is dependent on the size of the void space a
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