A general model for collaboration networks

In this paper, we propose a general model for collaboration networks. Depending on a single free parameter "{\bf preferential exponent}", this model interpolates between networks with a scale-free and an exponential degree distribution. The degree distribution in the present networks can be roughly classified into four patterns, all of which are observed in empirical data. And this model exhibits small-world effect, which means the corresponding networks are of very short average distance and highly large clustering coefficient. More interesting, we find a peak distribution of act-size from empirical data which has not been emphasized before of some collaboration networks. Our model can produce the peak act-size distribution naturally that agrees with the empirical data well.Comment: 10 pages, 10 figure

4-(3-Carb­oxy­phen­yl)pyridinium nitrate

In the title salt, C12H10NO2 +·NO3 −, the dihedral angle between the pyridine ring and the benzene ring of the 4-(3-carb­oxy­phen­yl)pyridinium cation is 30.14 (2)°. Inversion-related pairs of cations are linked into dimers by pairs of O—H⋯O hydrogen bonds. Pairs of dimers are linked by N—H⋯O and C—H⋯O hydrogen bonds involving nitrate anions as acceptors, generating supra­molecular chains along the diagonal of the bc plane

Easily Tunable Membrane Thickness of Microcapsules by Using a Coordination Assembly on the Liquid-Liquid Interface

A model solvent, 1,3,5-trimethylbenzene, was encapsulated using coordination assembly between metal ions and tannic acid to reveal the deposition of coordination complexes on the liquid-liquid interface. The deposition was confirmed by zeta potential, energy dispersive spectroscopy and X-ray photoelectron spectroscopy. Scanning electron microscopy and transmission electron microscopy were integrated to characterize the microcapsules (MCs). According to atomic force microscopy height analysis, membrane thickness of the MCs increased linearly with sequential deposition. For MCs prepared using the Fe3+-TA system, the average membrane thicknesses of MCs prepared with 2, 4, 6, and 8 deposition cycles were determined as 31.3 ± 4.6, 92.4 ± 15.0, 175.4 ± 22.1, and 254.8 ± 24.0 nm, respectively. Dissolution test showed that the release profiles of all the four tested MCs followed Higuchi kinetics. Membrane thicknesses of MCs prepared using the Ca2+-TA system were much smaller. We can easily tune the membrane thickness of the MCs by adjusting metal ions or deposition cycles according to the application requirements. The convenient tunability of the membrane thickness can enable an extensive use of this coordination assembly strategy in a broad range of applications

Origin of increased helium density inside bubbles in Ni(1-x)Fex alloys

Due to virtually no solubility, He atoms implanted or created inside materials tend to form bubbles, which are known to damage material properties through embrittlement. Higher He density in nano-sized bubbles was observed both experimentally and computationally in Ni(100-x)Fex-alloy samples compared to Ni. The bubbles in the Ni(100-x)Fex-alloys were observed to be faceted, whereas in elemental Ni they were more spherical. Molecular dynamics simulations showed that stacking fault structures formed around bubbles at maximum He density. Higher Fe concentrations stabilize stacking fault structures, suppress evolution of dislocation network around bubbles and suppress complete dislocation emission, leading to higher He density. (C) 2020 Acta Materialia Inc. Published by Elsevier Ltd.Peer reviewe

Ultrasound-assisted degradation of a new bacterial exopolysaccharide WL-26 from Sphingomonas sp.

Ultrasonic degradation of a new exopolysaccharide WL-26 from Sphingomonas sp. was made over the frequency range 200 to 1200 Hz and polymer concentrations of 3, 5, 10 and 20 g/L using high performance anion exchange pulsed-amperometric detection chromatography (HPAEC–PAD) and infrared spectroscopy. Sonication was more efficient with less concentrated polysaccharide solutions, high ultrasonic frequency, long duration of ultrasonic irradiation and degradation continued until a limiting molecular weight was attained. Results show that HPAEC–PAD revealed WL-26 to be an acidic polysaccharide composed of rhamnose, glucose, mannose, galactose and glucuronic acid in the molar ratio of 10:9:3:1:3 distinctly different from welan gum which does not contain galactose.Key words: Exopolysaccharide WL-26, ultrasonic degradation, infrared spectroscopy