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151.
文章认为R4和高速下行数据接入(HSDPA)的混合组网方式是目前比较合理的组网方式,可以减少建设成本,并降低管理维护和优化的复杂度,是主流运营商倾向的组网方式。文章提出通过理论计算结合系统级仿真手段可以对基于TD-SCDMA的R4与HSDPA业务混合组网前后系统性能进行对比研究,并提出通过优化HSDPA业务信道发射功率、调度算法、无线资源管理(RRM)算法等多种手段可以提升混合组网后系统性能。 相似文献
152.
153.
The design, fabrication, and electrical characteristics of the 4H-SiC JBS diode with a breakdown voltage higher than 10 kV are presented. 60 floating guard rings have been used in the fabrication. Numerical simulations have been performed to select the doping level and thickness of the drift layer and the effectiveness of the edge termination technique. The n-type epilayer is 100 μm in thickness with a doping of 6 × 10^14 cm^-3. The on-state voltage was 2.7 V at JF = 13 A/cm^2. 相似文献
154.
We investigate the phenomena of spontaneous symmetry breaking
for φ4 model on a square lattice in the parameter space by using
the potential importance sampling method, which was proposed by Milchev,
Heermann, and Binder [J. Stat. Phys. 44 (1986) 749]. The critical
values of the parameters allow us to determine the phase diagram of the
model. At the same time, some relevant quantities such as
susceptibility and specific heat are also obtained. 相似文献
155.
以处理后的脱硫石膏为原料,在H2SO4-H2O体系中以Cu(NO3)2为晶形控制剂采用水热法制备脱硫石膏晶须,探讨了Cu(NO3)2对脱硫石膏晶须生长的影响机理。结果表明:Cu(NO3)2对脱硫石膏有明显促溶作用,其中Cu2+可减小溶液中各离子的活度系数,使溶液中的Ca2+浓度增大。NO-3通过静电作用在Ca2+周围聚集并对SO2-4产生屏蔽作用,导致脱硫石膏继续溶解并使Ca2+和SO2-4的浓度处于相对稳定状态,有利于半水脱硫石膏晶体的形核与生长。此外,Cu2+还可在晶须的生长过程中选择性吸附在晶须表面,生成CuSO4,促进了脱硫石膏的结晶生长,最终在Cu(NO3)2用量为2.0%(质量分数)时制备的脱硫石膏晶须长径比约为73。 相似文献
156.
157.
Bin-Long Sun Ying-Ying Wang Sen Yang Min-Ting Tu Ying-Ying Shao Yi Hua Yi Zhou Cheng-Xia Tan 《Molecules (Basel, Switzerland)》2022,27(12)
To develop new compounds with high activity, broad spectrum and low-toxicity, 17 benzamides substituted with quinoline-linked 1,2,4-oxadiazole were designed using the splicing principle of active substructures and were synthesized. The biological activities were evaluated against 10 fungi, indicating that some of the synthetic compounds showed excellent fungicidal activities. For example, at 50 mg/L, the inhibitory activity of 13p (3-Cl-4-Cl substituted, 86.1%) against Sclerotinia sclerotiorum was superior to that of quinoxyfen (77.8%), and the inhibitory activity of 13f (3-CF3 substituted, 77.8%) was comparable to that of quinoxyfen. The fungicidal activities of 13f and 13p to Sclerotinia sclerotiorum were better than that of quinoxyfen (14.19 mg/L), with EC50 of 6.67 mg/L and 5.17 mg/L, respectively. Furthermore, the acute toxicity of 13p was 19.42 mg/L, classifying it as a low-toxic compound. 相似文献
158.
159.
As a global health problem, liver fibrosis still does not have approved treatment. It was proved that N-(3,4,5-trichlorophenyl)-2(3-nitrobenzenesulfonamide) benzamide (IMB16-4) has anti-hepatic fibrosis activity. However, IMB16-4 displays poor water solubility and poor bioavailability. We are devoted to developing biodegraded liposome-coated polymeric nanoparticles (LNPs) as IMB16-4 delivery systems for improving aqueous solubility, cellular uptake, and anti-fibrotic effects. The physical states of IMB16-4−LNPs were analyzed using a transmission electron microscope (TEM), high-performance liquid chromatography (HPLC), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and differential scanning calorimeter (DSC). The results show that IMB16-4−LNPs increased the drug loading compared to liposomes and enhanced cellular uptake behavior compared with IMB16-4−NPs. In addition, IMB16-4−LNPs could repress the expression of hepatic fibrogenesis-associated proteins, indicating that IMB16-4−LNPs exhibited evident anti-fibrotic effects. 相似文献
160.
Xuan Zhao Jiqing Fang Yu Jia Zi Wu Meihui Zhang Mingyu Xia Jinhua Dong 《Molecules (Basel, Switzerland)》2022,27(11)
A series of 1,7-diphenyl-1,4-heptadien-3-ones with various substituents (HO-, CH3O-, CH3-, Cl-) on the phenyl rings were synthesized and evaluated for anti-neuroinflammatory effects in LPS-stimulated BV2 microglia. The pharmacological results showed that the target compounds bearing methoxy groups greatly inhibited LPS-induced NO release, and that the active compounds CU-19 and CU-21 reduced the level of NO, TNF-α, IL-6 and PGE-2, downregulated the expression of COX-2 and iNOS in LPS-stimulated BV2 cells. A study of the mechanism of action revealed that CU-19 and CU-21 inhibited the nuclear translocation of NF-κB and phosphorylation of MAPKs (ERK, JNK, and p38). A preliminary pharmacokinetic study in rats revealed that the pharmacokinetic properties of CU-19 and CU-21 were dramatically ameliorated in comparison with the pharmacokinetic properties of curcumin. 相似文献