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Although higher intakes of specific trans-fatty acids and conjugated linoleic were associated with an increased risk of ASCVD, the same cannot be said for all other fat classes. This work suggests that care must be taken when drawing general conclusions regarding the health effects of dietary individual fatty acids.
Abstract The initial rates of the enzyme‐catalyzed hydrolysis of over 50 N‐acylamino acids and analogues and the resolution of 11 amino acids, e.g. (I), are reported.
On the basis of elastodynamic stress fields for singular crack and nonsingular slip‐weakening models of propagating rupture, we develop preliminary answers to such questions as follows: If a rupturing fault is intersected by another, providing a possible bend in the failure path, when will stressing be consistent with rupture along the bend? What secondary fault locations and orientations, in a damaged region bordering a major fault, will be stressed to failure by the main rupture? Stresses that could initiate rupture on a bend are shown to increase dramatically with crack speed, especially near the limiting speed (Rayleigh for mode II, shear for mode III). Whether a bend path, once begun, can be continued to larger scales depends on principal stress directions and ratios in the prestress field. Conditions should often be met in mode II for which bend paths encouraged by stressing very near the rupture tip are discouraged by the larger‐scale stressing, a basis for intermittent rupture propagation and spontaneous arrest. Secondary failure in the damage zone likewise increases markedly as the limiting speed is approached. Such may make the fracture energy much greater than for slip on a single surface. The extent of secondary faulting is strongly affected by prestress directions and the ratio of residual to peak strength. For mode II, prestress controls whether activation occurs primarily on the extensional side, which we show to be the typical case, or on the compressional side too. Natural examples are consistent with the concepts developed.
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ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDetermination of enantiomeric purity of polar substrates with chiral lanthanide NMR shift reagents in polar solventsLinda M. Sweeting, Debbie C. Crans, and George M. WhitesidesCite this: J. Org. Chem. 1987, 52, 11, 2273–2276Publication Date (Print):May 1, 1987Publication History Published online1 May 2002Published inissue 1 May 1987https://pubs.acs.org/doi/10.1021/jo00387a030https://doi.org/10.1021/jo00387a030research-articleACS PublicationsRequest reuse permissionsArticle Views590Altmetric-Citations51LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Cyclic morphological instabilities in the thermally grown oxide (TGO) represent a source of failure in some thermal barrier systems. Observations and simulations have indicated that several factors interact to cause these instabilities to propagate: (i) thermal cycling; (ii) thermal expansion misfit; (iii) oxidation strain; (iv) yielding in the TGO and the bond coat; and (v) initial geometric imperfections. This study explores a fundamental understanding of the propagation phenomenon by devising a spherically symmetric model that can be solved analytically. The applicability of this model is addressed through comparison with simulations conducted for representative geometric imperfections and by analogy with the elastic/plastic indentation of a half space. Finite element analysis is used to confirm and extend the model. The analysis identifies the dependencies of the instability on the thermo-mechanical properties of the system. The crucial role of the in-plane growth strain is substantiated, as well as the requirement for bond coat yielding. It is demonstrated that yielding of the TGO is essential and is, in fact, the phenomenon that differentiates between cyclic and isothermal responses.
Semiconductor nanowires represent unique materials for exploring phenomena at the nanoscale. Developments in nanowire growth have led to the demonstration of a wide range of nanowire materials with precise control of composition, morphology, and electrical properties, and it is believed that this excellent control together with small channel size could yield device performance exceeding that obtained using top-down techniques. Here, we review advances in chemically synthesized semiconductor nanowires as nanoelectronic devices. We first introduce basic nanowire field-effect transistor structures and review results obtained from both p- and n-channel homogeneous composition nanowires. Second, we describe nanowire heterostructures, show that by using nanowire heterostructures, several limiting factors in homogeneous nanowire devices can be mitigated, and demonstrate that nanowire transistor performance can reach the ballistic limit and exceed state-of-the-art planar devices. Third, we discuss basic methods for organization of nanowires necessary for fabricating arrays of device and circuits. Fourth, we introduce the concept of crossbar nanowire circuits, discuss results for both transistor and nonvolatile switch devices, and describe unique approaches for multiplexing/demultiplexing enabled by synthetically coded nanowire. Fifth, we discuss the unique application of thin-film nanowire transistor arrays on low-cost substrates and illustrate this with results for relatively high-frequency ring oscillators and completely transparent device arrays. Finally, we describe 3-D heterogeneous integration that is uniquely enabled by multifunctional nanowires within a bottom-up approach.
Scanning tunneling microscopy has been used to characterize the surface structure of the KHgC4 (stage 1) and KHgC8 (stage 2) graphite intercalation compounds. Images of the stage 1 and stage 2 materials exhibit a new commensurate 2×2 superlattice in addition to the centered hexagonal lattice observed in images of pristine graphite. Consideration of the intercalant layer structure and previous studies of stage 1 (MC8) and stage 2 (MC24) alkali metal graphite intercalation compounds (GICs) indicate that the 2×2 superlattice is due to a modulation of the surface carbon layer density of states by the periodic (2×2) potential of the potassium ions. In addition, a new orthorhombic superlattice, a=b=0.89 nm and <a−b≂89°, has been observed in images of the stage 1 KHgC4 material. Possible origins of this novel superstructure are discussed.