Proposal for measuring new transverse momentum dependent parton distributions g1Tg_{1T} and h1L⊥h_{1L}^\perp through semi-inclusive deep inelastic scattering

We calculate $g_{1T}$ and $h_{1L}^\perp$, two of the eight leading twist transverse momentum dependent parton distributions (TMDs), in the light-cone quark-diquark model. The new TMDs can be measured through semi-inclusive deep inelastic scattering (SIDIS). We present predictions of the single and double spin asymmetries related to $g_{1T}$ and $h_{1L}^\perp$ in SIDIS at HERMES, COMPASS, and JLab kinematics respectively.Comment: 14 latex pages, 7 figures, final version for journal publicatio

Pretzelosity h1T⊥h_{1T}^{\perp} and quark orbital angular momentum

We calculate the pretzelosity distribution ($h_{1T}^{\perp}$), which is one of the eight leading twist transverse momentum dependent parton distributions (TMDs), in the light-cone formalism. We find that this quantity has a simple relation with the quark orbital angular momentum distribution, thus it may provide a new possibility to access the quark orbital angular momentum inside the nucleon. The pretzelosity distribution can manifest itself through the $\sin(3\phi_h-\phi_S)$ asymmetry in semi-inclusive deep inelastic scattering process. We calculate the $\sin(3\phi_h-\phi_S)$ asymmetry at HERMES, COMPASS and JLab kinematics, and present our prediction on different targets including the proton, deuteron and neutron targets. Inclusion of transverse momentum cut in data analysis could significantly enhance the $\sin(3\phi_h-\phi_S)$ asymmetry for future measurements.Comment: 20 latex pages, 7 figures, to appear in PR

Azimuthal asymmetries in single polarized proton-proton Drell-Yan processes

We study the azimuthal asymmetries in proton-proton Drell-Yan processes with one incident proton being transversely or longitudinally polarized. We consider particularly the asymmetries contributed by the leading-twist chiral-odd quark distributions. We analyze the asymmetries with $\sin(2\phi+\phi_S)$ and $\sin(2\phi-\phi_S)$ modulations in transverse single polarized $p^\uparrow p$ Drell-Yan and $\sin2\phi$ asymmetries in longitudinal single polarized $p^\rightarrow p$ Drell-Yan at RHIC, J-PARC, E906 (Fermi Lab) and NICA (JINR). We show that the measurements of the asymmetries in those facilities can provide valuable information of the chiral-odd structure of the nucleon both in the valence and sea regions.Comment: 12 latex pages, 7 figures. Final version to appear in PR

Three-dimensional parton distribution functions g1Tg_{1T} and h1L⊥h_{1L}^\perp in the polarized proton-antiproton Drell-Yan process

We present predictions of the unweighted and weighted double spin asymmetries related to the transversal helicity distribution $g_{1T}$ and the longitudinal transversity distribution $h_{1L}^\perp$, two of eight leading-twist transverse momentum dependent parton distributions (TMDs) or three-dimensional parton distribution functions (3dPDFs), in the polarized proton-antiproton Drell-Yan process at typical kinematics on the Facility for Antiproton and Ion Research (FAIR). We conclude that FAIR is ideal to access the new 3dPDFs towards a detailed picture of the nucleon structure.Comment: 6 latex pages, 5 figures, version for publication in EPJ

Interfacial Characteristics of Boron Nitride Nanosheet/Epoxy Resin Nanocomposites: A Molecular Dynamics Simulation

The interface between nanofillers and matrix plays a key role in determining the properties of nanocomposites, but the interfacial characteristics of nanocomposites such as molecular structure and interaction strength are not fully understood yet. In this work, the interfacial features of a typical nanocomposite, namely epoxy resin (EP) filled with boron nitride nanosheet (BNNS) are investigated by utilizing molecular dynamics simulation, and the effect of surface functionalization is analyzed. The radial distribution density (RDD) and interfacial binding energy (IBE) are used to explore the structure and bonding strength of nanocomposites interface. Besides, the interface compatibility and molecular chain mobility (MCM) of BNNS/EP nanocomposites are analyzed by cohesive energy density (CED), free volume fraction (FFV), and radial mean square displacement (RMSD). The results indicate that the interface region of BNNS/EP is composed of three regions including compact region, buffer region, and normal region. The structure at the interfacial region of nanocomposite is more compact, and the chain mobility is significantly lower than that of the EP away from the interface. Moreover, the interfacial interaction strength and compatibility increase with the functional density of BNNS functionalized by CH3–(CH2)4–O– radicals. These results adequately illustrate interfacial characteristics of nanocomposites from atomic level

Optimization of Antenna Array Deployment for Partial Discharge Localization in Substations by Hybrid Particle Swarm Optimization and Genetic Algorithm Method

A radio frequency antenna array was adopted to localize partial discharge (PD) sources in an entire substation. The deployment of an antenna array is a significant factor affecting the localization accuracy, and the array needs to be carefully selected. In this work, a hybrid method of particle swarm optimization (PSO) and a genetic algorithm (GA) is proposed to optimize the array deployment. A direction-of-arrival (DOA) estimation algorithm applicable to arbitrary array configurations is firstly presented. The Cramér-Rao lower bound (CRLB) was employed to evaluate the localization accuracy of different arrays, and two objective functions characterizing the estimation errors of coordinates and the DOA are proposed. With the goal of minimizing the objective functions, the array deployments for the coordinate and DOA localizations were optimized by using the hybrid PSO/GA algorithm. Using the developed method, optimal antenna configurations for different constraint areas, aspect ratios, and numbers of sensors were investigated. The results indicate that the optimal deployments for coordinate and DOA estimations are different; specifically speaking, superior DOA performance is achieved when all antennas are placed on the outer boundary of the constraint area while part of the antennas in the optimal coordinate array are placed in the middle position

Improved Rotor Braking Protection Circuit and Self-Adaptive Control for DFIG during Grid Fault

This paper introduces an improved rotor braking protection circuit configuration and the corresponding self-adaptive control strategy to enhance the low voltage ride-through (LVRT) capability of the doubly-fed induction generator (DFIG). The proposed protection circuit consists of a crowbar circuit and a series rotor braking resistor array, which guarantees the safe operation of wind generators under the LVRT. Moreover, to adapt the proposed protection and further enhance the performance of the improved configuration, a corresponding self-adaptive control strategy is presented, which regulates the rotor braking resistor and protection exiting time automatically through calculating the rotor current in the fault period. The LVRT capability and transient performance of the DFIG by using the proposed method is tested with simulation. Compared with the conventional crowbar protection or the fixed rotor braking protection, the proposed protection and the control strategy present several advantages, such as retaining the control of the rotor side converter, avoiding repeated operation of the protection and accelerating the damping of stator flux linkage during a grid fault

Engineered bone marrow mesenchymal stem cell-derived exosomes loaded with miR302 through the cardiomyocyte specific peptide can reduce myocardial ischemia and reperfusion (I/R) injury

Abstract Background MicroRNA (miRNA)-based therapies have shown great potential in myocardial repair following myocardial infarction (MI). MicroRNA-302 (miR302) has been reported to exert a protective effect on MI. However, miRNAs are easily degraded and ineffective in penetrating cells, which limit their clinical applications. Exosomes, which are small bioactive molecules, have been considered as an ideal vehicle for miRNAs delivery due to their cell penetration, low immunogenicity and excellent stability potential. Herein, we explored cardiomyocyte-targeting exosomes as vehicles for delivery of miR302 into cardiomyocyte to potentially treat MI. Methods To generate an efficient exosomal delivery system that can target cardiomyocytes, we engineered exosomes with cardiomyocyte specific peptide (CMP, WLSEAGPVVTVRALRGTGSW). Afterwards, the engineered exosomes were characterized and identified using transmission electron microscope (TEM) and Nanoparticle Tracking Analysis (NTA). Later on, the miR302 mimics were loaded into the engineered exosomes via electroporation technique. Subsequently, the effect of the engineered exosomes on myocardial ischemia and reperfusion (I/R) injury was evaluated in vitro and in vivo, including MTT, ELISA, real-time quantitative polymerase chain reaction (PCR), western blot, TUNNEL staining, echocardiogram and hematoxylin and eosin (HE) staining. Results Results of in vitro experimentation showed that DSPE-PEG-CMP-EXO could be more efficiently internalized by H9C2 cells than unmodified exosomes (blank‐exosomes). Importantly, compared with the DSPE-PEG-CMP-EXO group, DSPE-PEG-CMP-miR302-EXO significantly upregulated the expression of miR302, while exosomes loaded with miR302 could enhance proliferation of H9C2 cells. Western blot results showed that the DSPE-PEG-CMP-miR302-EXO significantly increased the protein level of Ki67 and Yap, which suggests that DSPE-PEG-CMP-miR302-EXO enhanced the activity of Yap, the principal downstream effector of Hippo pathway. In vivo, DSPE-PEG-CMP-miR302-EXO improved cardiac function, attenuated myocardial apoptosis and inflammatory response, as well as reduced infarct size significantly. Conclusion In conclusion, our findings suggest that CMP-engineered exosomes loaded with miR302 was internalized by H9C2 cells, an in vitro model for cardiomyocytes coupled with potential enhancement of the therapeutic effects on myocardial I/R injury