基于复杂网络理论的多直流馈入受端电网优化分区方法

提出一种适用于基于复杂网络理论的多直流馈入受端电网多目标优化分区方法。利用复杂网络理论分析电网的复杂网络特性和物理特性本质,构建加权模块度指标和平均输电距离指标,以评价网络分区质量和电网输电效率。考虑电网分区对多直流馈入系统的影响,采用加权多馈入短路比(multi-feed short-circuit ratio, MISCR)量化受端电网强度,建立电网分区方案评价指标集合。以最大化加权模块度和MISCR、最小化平均输电距离为目标,构建三目标优化模型,通过工程经验削减分区方案可行域,并基于NSGA-Ⅱ算法进行求解。以某省级电网为例,对比分析了所提方法的有效性。算例分析结果表明,所提方法具有更好的综合分区效果,更适用于多直流馈入受端电网。     

Prediction of Commuter Vehicle Demand Torque Based on Historical Speed Information

The development of vehicle-to-everything and cloud computing has brought new opportunities and challenges to the automobile industry. In this paper, a commuter vehicle demand torque prediction method based on historical vehicle speed information is proposed, which uses machine learning to predict and analyze vehicle demand torque. Firstly, the big data of vehicle driving is collected, and the driving data is cleaned and features extracted based on road information. Then, the vehicle longitudinal driving dynamics model is established. Next, the vehicle simulation simulator is established based on the longitudinal driving dynamics model of the vehicle, and the driving torque of the vehicle is obtained. Finally, the travel is divided into several acceleration-cruise-deceleration road pairs for analysis, and the vehicle demand torque is predicted by BP neural network and Gaussian process regression.     

Electroless Plating of Copper on Fluorinated Polyimide Films Modified by Plasma Graft Copolymerization and UV‐induced Graft Copolymerization with 4‐Vinylpyridine

Surface modification of two types of fluorinated polyimide (FPI) films, either by plasma polymerization and deposition of 4‐vinylpyridine (4VP) or by UV‐induced graft copolymerization with 4VP under atmospheric conditions, was carried out for adhesion enhancement with the electrolessly deposited copper. X‐ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) results revealed that the pyridine groups in the plasma polymerized 4VP (pp‐4VP) layer could be preserved to a large extent under proper glow discharge conditions. The grafted 4VP layer with well‐preserved pyridine groups was used not only as the chemisorption sites for the palladium complexes (without the need for prior sensitization by SnCl₂) during the electroless plating of copper, but also as an adhesion promotion layer for the electrolessly deposited copper. The T‐peel adhesion strength of the electrolessly deposited copper with both the 4VP plasma‐polymerized FPI (pp‐4VP‐FPI) film and the 4VP graft‐copolymerized FPI (4VP‐g‐FPI) film was much higher than that of the electrolessly deposited copper with the pristine or the Ar plasma‐treated FPI films. The high adhesion strength between the electrolessly deposited copper and the surface‐modified FPI film was attributed to the fact that the plasma‐polymerized and the UV graft‐copolymerized 4VP chains were covalently tethered on the FPI surfaces, as well as the fact that these grafted 4VP polymer chains were spatially and reactively distributed into the copper matrix.

     

Radial Liquid Dispersion and Bubble Distribution in Three‐Phase Circulating Fluidized Beds

The liquid dispersion and bubble distribution in the radial direction have been investigated in the riser of a three‐phase circulating fluidized bed whose diameter is 0.102m and 3.5m in height. Effects of gas and liquid velocities and solid circulation rate have been determined. It has been found that the radial distribution of bubbles is related closely to the liquid dispersion in the radial direction. The size and rising velocity of bubbles tend to increase as the radial position approaches to the center of the riser. The bubble size increases with increasing U_G, but it decreases with increasing U_L or G_S in all radial positions. The radial dispersion coefficient of the liquid phase increases with increasing U_G or G_S, however, it tends to decrease with increasing U_L. The value of Dr has been well correlated in terms of dimensionless groups based on the isotropic turbulence model.     

Preparation and properties of polyelectrolyte complex sponges composed of hyaluronic acid and chitosan and their biological behaviors

Polyelectrolyte complexes (PECs) composed of chitosan and hyaluronic acid (HA) were prepared in various pH regions and at different weight ratios. At low pHs, there was a strong ionic interaction between NH groups in chitosan and both COO^? and COOH groups in HA due to the deprotonation of HA, whereas weak linkages were formed at high pHs because only the carboxyl groups of HA could interact with NH groups in chitosan. The formation of PECs resulted in a decrease in the crystallinity and thermal stability caused by the interactions between polyions. With variations in the degree of ionization of polyions at various pH conditions, novel PEC sponges were prepared by the freeze drying of PEC solutions. Furthermore, for the evaluation of the wound‐healing effect of PEC sponges with or without an antimicrobial agent (silver sulfadiazine), they were applied to a full‐skin defect of a Wistar rat in vivo. The histology and computerized morphometric analysis of the epidermal healing confirmed the proliferation of fibroblasts in the wound bed and a distinct reduction in infectious agents. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 925–932, 2003     

Flow-induced voltage generation over monolayer graphene in the presence of herringbone grooves

While flow-induced voltage over a graphene layer has been reported, its origin remains unclear. In our previous study, we suggested different mechanisms for different experimental configurations: phonon dragging effect for the parallel alignment and an enhanced out-of-plane phonon mode for the perpendicular alignment (Appl. Phys. Lett. 102:063116, 2011). In order to further examine the origin of flow-induced voltage, we introduced a transverse flow component by integrating staggered herringbone grooves in the microchannel. We found that the flow-induced voltage decreased significantly in the presence of herringbone grooves in both parallel and perpendicular alignments. These results support our previous interpretation.     

Immobilization of pamidronic acids on the nanotube surface of titanium discs and their interaction with bone cells

Self-assembled layers of vertically aligned titanium nanotubes were fabricated on a Ti disc by anodization. Pamidronic acids (PDAs) were then immobilized on the nanotube surface to improve osseointegration. Wide-angle X-ray diffraction, X-ray photoelectron microscopy, and scanning electron microscopy were employed to characterize the structure and morphology of the PDA-immobilized TiO₂ nanotubes. The in vitro behavior of osteoblast and osteoclast cells cultured on an unmodified and surface-modified Ti disc was examined in terms of cell adhesion, proliferation, and differentiation. Osteoblast adhesion, proliferation, and differentiation were improved substantially by the topography of the TiO₂ nanotubes, producing an interlocked cell structure. PDA immobilized on the TiO₂ nanotube surface suppressed the viability of the osteoclasts and reduced their bone resorption activity.     

Reconstructing a Flavodoxin Oxidoreductase with Early Amino Acids

Primitive proteins are proposed to have utilized organic cofactors more frequently than transition metals in redox reactions. Thus, an experimental validation on whether a protein constituted solely by early amino acids and an organic cofactor can perform electron transfer activity is an urgent challenge. In this paper, by substituting “late amino acids (C, F, M, T, W, and Y)” with “early amino acids (A, L, and V)” in a flavodoxin, we constructed a flavodoxin mutant and evaluated its characteristic properties. The major results showed that: (1) The flavodoxin mutant has structural characteristics similar to wild-type protein; (2) Although the semiquinone and hydroquinone flavodoxin mutants possess lower stability than the corresponding form of wild-type flavodoxin, the redox potential of double electron reduction E_m,7 (fld) reached −360 mV, indicating that the flavodoxin mutant constituted solely by early amino acids can exert effective electron transfer activity.     

Femtosecond laser modification of an array of vertically aligned carbon nanotubes intercalated with Fe phase nanoparticles

Femtosecond lasers (FSL) are playing an increasingly important role in materials research, characterization, and modification. Due to an extremely short pulse width, interactions of FSL irradiation with solid surfaces attract special interest, and a number of unusual phenomena resulted in the formation of new materials are expected. Here, we report on a new nanostructure observed after the interaction of FSL irradiation with arrays of vertically aligned carbon nanotubes (CNTs) intercalated with iron phase catalyst nanoparticles. It was revealed that the FSL laser ablation transforms the topmost layer of CNT array into iron phase nanospheres (40 to 680 nm in diameter) located at the tip of the CNT bundles of conical shape. Besides, the smaller nanospheres (10 to 30 nm in diameter) are found to be beaded at the sides of these bundles. Some of the larger nanospheres are encapsulated into carbon shells, which sometime are found to contain CNTs. The mechanism of creation of such nanostructures is proposed.     

Conjugated polymer mediated synthesis of nanoparticle clusters and core/shell nanoparticles

Two water soluble conjugated polymers, poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and ammonium ion stabilized poly(phenylene vinylene) (P2), are found to be able to reduce noble metal ions to zero-valent metals via a direct chemical deposition technique. Au nanoparticle clusters can be obtained through reduction of Au³⁺ ions by PEDOT:PSS and the electronic coupling between them can be controlled by HAuCl₄ concentration. Core/shell Ag/polymer nanostructures are prepared from reduction of Ag⁺ ions by P2, which have a ppb detection limit for 4-MBA using surface-enhanced Raman spectroscopy (SERS). This conjugated polymer mediated synthesis of metal nanoparticles may open a new avenue for fabricating nanomaterials and nanocomposites with tunable optical properties that are dominated by their structure and electronic coupling between nanoparticles.