基于L1正则化的随机梁式结构静力损伤识别方法

提出了一种结合摄动法和L1正则化方法的随机梁式结构静力损伤识别方法。考虑初始模型误差和测量误差的影响,建立了关于随机损伤指数的控制方程,并将摄动法和L1正则化方法相结合,对随机损伤指数的控制方程进行求解,进而从概率的角度对结构的损伤进行识别。损伤试验结果表明,和传统的最小二乘求解法相比,本文方法能够更为准确地识别多处局部损伤的位置及大小,对实际结构损伤检测具有较好的参考价值。     

振型归一化对梁结构柔度曲率损伤指标的影响

结构柔度矩阵需由质量矩阵归一化振型获得,而质量矩阵归一化振型难以直接测得,限制了柔度曲率类损伤指标的应用。为分析振型归一化方法对梁结构柔度曲率类损伤指标的影响,根据梁结构的刚度、弯矩和位移曲率的关系,建立了均布荷载作用下结构损伤前后位移曲率与损伤程度的理论表达式,实现定量分析均匀荷载面曲率结构损伤程度。提出P-范数振型归一化方法,通过均匀荷载面曲率指标推导了振型质量矩阵归一化系数差x_α与损伤程度的关系。以三跨连续梁算例对理论进行了验证,结果表明,损伤程度定量指标效果良好,不同P-范数振型归一化方法下,损伤程度的偏差可由2x_α估算;2-范数振型归一化方法的损伤识别结果与质量矩阵振型归一化结果最接近,故当无法获得质量矩阵归一化振型时,可采用2-范数归一化振型代替。     

Peridynamic modeling of pitting corrosion damage

In this paper we introduce a peridynamic model for the evolution of damage from pitting corrosion capable of capturing subsurface damage. We model the anodic reaction in corrosion processes (in which electroplating is negligible) as an effective peridynamic diffusion process in the electrolyte/solid system coupled with a phase-change mechanism that allows for autonomous evolution of the moving interface. In order to simulate creation of subsurface damage, we introduce a corrosion damage model based on a stochastic relationship that connects the concentration in the metal to the damage of peridynamic mechanical-bonds that are superposed onto diffusion-bonds. We study convergence of this formulation for diffusion-dominated stage. The model leads to formation of a subsurface damage layer, seen in experiments. We validate results against experiments on pit growth rate and polarization data for pitting corrosion. We extend the 1D model to the 2D and 3D, and introduce a new damage-dependent corrosion model to account for broken mechanical bonds that enhance the corrosion rate. This coupled model can predict the pit shape and damage profile in materials with microstructural heterogeneities, such as defects, interfaces, inclusions, and grain boundaries.     

Can a Six‐Letter Alphabet Increase the Likelihood of Photochemical Assault to the Genetic Code?

In 2014, two unnatural nucleosides, d5SICS and dNaM, were shown to selectively base pair and replicate with high fidelity in a modified strain of E. coli, thus effectively expanding its genetic alphabet from four to six letters. More recently, a significant reduction in cell proliferation was reported in cells cultured with d5SICS, and putatively with dNaM, upon exposure to brief periods of near‐visible radiation. The photosensitizing properties of the lowest‐energy excited triplet state of both d5SICS and dNaM were implicated in their cytotoxicity. Importantly, however, the excited‐state mechanisms by which near‐visible excitation populates the triplet states of d5SICS and dNaM are currently unknown. In this study, steady‐state and time‐resolved spectroscopies are combined with quantum‐chemical calculations in order to reveal the excited‐state relaxation mechanisms leading to efficient population of the triplet states in these unnatural nucleosides in solution. It is shown that excitation of d5SICS or dNaM with near‐visible light leads overwhelmingly to ultrafast population of their triplet states on the femtosecond time scale. The results presented in this work lend strong support to the proposal that photoexcitation of these unnatural nucleosides can accelerate oxidatively generated damage to DNA and other biomolecules within the cellular environment.     

Molecular dynamics simulations of displacement cascades in Fe-10%Cr systems

Molecular dynamics simulations of the displacement cascades in Fe-10%Cr systems are used to simulate the primary knocked-on atom events of the irradiation damage at temperatures 300,600,and 750 K with primary knockedon atom energies between 1 and 15 keV.The results indicate that the vacancies produced by the cascade are all in the central region of the displacement cascade.During the cascade,all recoil Fe and Cr atoms combine with each other to form Fe-Cr or Fe-Fe interstitial dumbbells as well as interstitial clusters.The number and the size of interstitial clusters increase with the energy of the primary knocked-on atom and the temperature.A few large clusters consist of a large number of Fe interstitials with a few Cr atoms,the rest are Fe-Cr clusters with small and medium sizes.The interstitial dumbbells of Fe-Fe and Fe-Cr are in the 111 and 110 series directions,respectively.     

Microstructure change in deuterium implanted CLAM steel induced by electron irradiation

As Reduced Activation Ferritic/Martensitic (RAFM) steel is considered the primary candidate for use as a structural material in fusion power reactors,many countries are developing different kinds of RAFM.China is developing new CLAM (China Low Activation Martensitic) steel.The study investigates microstructural changes in CLAM steel implanted with deuterium ions induced by 1250 keV electron irradiation from R.T.to 873 K,and observes both the growth and shrinkage of the defect clusters produced by deuterium ...     

Polypyridyl-Based Copper Phenanthrene Complexes: Combining Stability with Enhanced DNA Recognition

We report a series of copper(II) artificial metallo-nucleases (AMNs) and demonstrate their DNA damaging properties and in-vitro cytotoxicity against human-derived pancreatic cancer cells. The compounds combine a tris-chelating polypyridyl ligand, di-(2-pycolyl)amine (DPA), and a DNA intercalating phenanthrene unit. Their general formula is Cu-DPA-N,N' (where N,N'=1,10-phenanthroline (Phen), dipyridoquinoxaline (DPQ) or dipyridophenazine (DPPZ)). Characterisation was achieved by X-ray crystallography and continuous-wave EPR (cw-EPR), hyperfine sublevel correlation (HYSCORE) and Davies electron-nuclear double resonance (ENDOR) spectroscopies. The presence of the DPA ligand enhances solution stability and facilitates enhanced DNA recognition with apparent binding constants (K_app) rising from 10⁵ to 10⁷ m ⁻¹ with increasing extent of planar phenanthrene. Cu-DPA-DPPZ, the complex with greatest DNA binding and intercalation effects, recognises the minor groove of guanine–cytosine (G-C) rich sequences. Oxidative DNA damage also occurs in the minor groove and can be inhibited by superoxide and hydroxyl radical trapping agents. The complexes, particularly Cu-DPA-DPPZ, display promising anticancer activity against human pancreatic tumour cells with in-vitro results surpassing the clinical platinum(II) drug oxaliplatin.     

Multiaxial mechanical behavior of aramid fibers and identification of skin/core structure from single fiber transverse compression testing

The transverse and longitudinal mechanical properties of aramid fibers like Kevlar? 29 (K29) fibers are strongly linked to their highly oriented structure. Mechanical characterization at the single fiber scale is challenging especially when the diameter is as small as 15 µm. Longitudinal tensile tests on single K29 fibers and single fiber transverse compression test (SFTCT) have been developed. Our approach consists of coupling morphological observations and mechanical experiments with SFTCT analysis by comparing analytical solutions and finite element modeling. New insights on the analysis of the transverse direction response are highlighted. Systematic loading/unloading compression tests enable to experimentally determine a transverse elastic limit. Taking account of the strong anisotropy of the fiber, the transverse mechanical response sheds light on a skin/core architecture. More importantly, results suggest that the skin of the fiber, typically representing a shell of one micrometer in thickness, has a transverse apparent modulus of 0.2 GPa. That is around more than fifteen times lower than the transverse modulus of 3.0 GPa in the core. By comparison, the measured longitudinal modulus is about 84 GPa. The stress distribution in the fiber is explored and the critical areas for damage initiation are discussed. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 374–384     

Modification of the lunar surface by solar wind ion bombardment

Trivalent osmium ions are substitutionally incorporated into aqueous precipitates and melt-grown single crystals of AgBr and AgC1. The ions are distributed between three structurally inequivalent lattice sites in both salts. From epr studies, we have inferred that these sites are distinguished by the arrangement of charge-compensating silver ion vacancies in the two closest cation subshells. The most reasonable dopant-vacancy configurations have been deduced from the epr data. These configurations persist up to at least 300 K, and are compared with those observed in other trivalent metal ion doped systems.