Numerical Simulation of Three Phase Displacement Characteristics of Foam Fluid In Homogeneous Porous Media

Foam technology has found wide applications in enhanced oil recovery and greenhouse geological storage. In this paper, a numerical simulate is carried out with the stochastic bubble population balance model on the foam three phase displacement process in a homogeneous oil/water/gas coexistence porous media of liquid. The effects of the maximum equilibrium bubble density nmax and the foam generation rate Kg on foam displacement process is mainly discussed. Numerical results indicate that the oil phase can be displaced well by foam fluid. Larger nmax values lead to higher apparent viscosity of foam and higher the pressure difference, and with the increase of Kg, the number of foam can reach a balance in a short distance, so it has better displacement effect on the oil phase components. The results obtained in this paper have a certain guiding role in understanding the enhanced oil recovery mechanism of foam fluid

A self-consistent method to analyze the effects of the positive Q-value neutron transfers on fusion

AbstractConsidering the present limitation of the need for external parameters to describe the nucleus–nucleus potential and the couplings in the coupled-channels calculations, this work introduces an improved method without adjustable parameter to overcome the limitation and then sort out the positive Q-value neutron transfers (PQNT) effects based on the CCFULL calculations. The corresponding analysis for Ca+Ca, S,Ca+Sn, and S,Ca+Zr provides a reliable proof and a quantitative evaluation for the residual enhancement (RE) related to PQNT. In addition, the RE for S32,Ca40+Zr94 shows an unexpected larger enhancement than S32,Ca40+Zr96 despite the similar multi-neutron transfer Q-values. This method should rather strictly test the fusion models and be helpful for excavating the underlying physics

Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization

Contemporary models of intrafibrillar mineralization mechanisms are established using collagen fibrils as templates without considering the contribution from collagen-bound apatite nucleation inhibitors. However, collagen matrices destined for mineralization in vertebrates contain bound matrix proteins for intrafibrillar mineralization. Negatively charged, high\u2013molecular weight polycarboxylic acid is cross-linked to reconstituted collagen to create a model for examining the contribution of collagen-ligand interaction to intrafibrillar mineralization. Cryogenic electron microscopy and molecular dynamics simulation show that, after cross-linking to collagen, the bound polyelectrolyte caches prenucleation cluster singlets into chain-like aggregates along the fibrillar surface to increase the pool of mineralization precursors available for intrafibrillar mineralization. Higher-quality mineralized scaffolds with better biomechanical properties are achieved compared with mineralization of unmodified scaffolds in polyelectrolyte-stabilized mineralization solution. Collagen-ligand interaction provides insights on the genesis of heterogeneously mineralized tissues and the potential causes of ectopic calcification in nonmineralized body tissues

Development of a metal-free black phosphorus/graphitic carbon nitride heterostructure for visible-light-driven degradation of indomethacin

The development of affordable and efficient technologies for the removal of pharmaceuticals and personal care products (PPCPs) from water has recently been the subject of extensive attention. In this study, a black phosphorus/graphitic carbon nitride (BP-g-C3N4) heterostructure is fabricated as an extremely active metal-free photocatalyst via a newly-developed exfoliation strategy. The BP-g-C3N4 shows an 11 times better decomposition rate of a representative PPCPs-type pollutant, indomethacin (IDM), compared to the widely used P25 TiO2 under real-sunlight illumination. Also, its visible-light activity is even better than that of the best photocatalysts previously developed, but only consumes 1/10-1/4 of the catalyst. The results show that BP performs a cocatalyst-like behavior to catalyze the generation of reactive oxygen species, thus speeding up the decomposition of IDM. In addition, the BP-g-C3N4 photocatalyst also exhibits excellent IDM removal efficiency in authentic water matrices (tap water, surface water, and secondarily treated sewage effluent). Large-scale application demonstration under natural sunlight further reveals the practicality of BP-g-C3N4 for real-world water treatment operations. Our work will open up new possibilities in the development of purely metal-free photocatalysts for "green" environmental remediation applications. (C) 2021 Elsevier B.V. All rights reserved.Environmental Biolog

Direct Measurements of the Branching Fractions for D0→K−e+νeD^0 \to K^-e^+\nu_e and D0→π−e+νeD^0 \to \pi^-e^+\nu_e and Determinations of the Form Factors f+K(0)f_{+}^{K}(0) and f+π(0)f^{\pi}_{+}(0)

The absolute branching fractions for the decays $D^0 \to K^-e ^+\nu_e$ and $D^0 \to \pi^-e^+\nu_e$ are determined using $7584\pm 198 \pm 341$ singly tagged $\bar D^0$ sample from the data collected around 3.773 GeV with the BES-II detector at the BEPC. In the system recoiling against the singly tagged $\bar D^0$ meson, $104.0\pm 10.9$ events for $D^0 \to K^-e ^+\nu_e$ and $9.0 \pm 3.6$ events for $D^0 \to \pi^-e^+\nu_e$ decays are observed. Those yield the absolute branching fractions to be $BF(D^0 \to K^-e^+\nu_e)=(3.82 \pm 0.40\pm 0.27)$ and $BF(D^0 \to \pi^-e^+\nu_e)=(0.33 \pm 0.13\pm 0.03)$. The vector form factors are determined to be $|f^K_+(0)| = 0.78 \pm 0.04 \pm 0.03$ and $|f^{\pi}_+(0)| = 0.73 \pm 0.14 \pm 0.06$. The ratio of the two form factors is measured to be $|f^{\pi}_+(0)/f^K_+(0)|= 0.93 \pm 0.19 \pm 0.07$.Comment: 6 pages, 5 figure