Electrophoretic deposition of CoFe2O4 films from aqueous suspensions

CoFe₂O₄ nano-particles with average size of ～40 nm were synthesized via the chemical coprecipitation method. PAMANH₄ was used as dispersant to improve the stability of aqueous suspensions. Zeta potential and sediment volumes were tested to study the effects of pH and dispersant amounts on the stability of suspensions. The most stable suspension was obtained when using 0.6 wt.% PAMANH₄ as dispersant at pH = 10. Conductivity results showed that thoroughly dispersed suspensions were formed after being ultrasonic agitated for 30 min. CoFe₂O₄ films on Al₂O₃/Pt substrates fabricated via EPD sintered at 1250 °C exhibited preferentially oriented structure. The XRD analyses showed (2 2 0) and (5 1 1) were the preferential orientations. Anisotropy was also observed in magnetic hysteresis loops. Stronger ferromagnetic effect was observed in the in-plane orientation, with saturation magnetization of ～290 emu/cm³.     

Preparation and properties of polymer-encapsulated phthalocyanine blue pigment via emulsion polymerization

Polymer-encapsulated phthalocyanine blue pigment dispersion was prepared with a polymerizable dispersant by emulsion polymerization method, and the effect of preparation conditions on the particle size of dispersion was investigated. Dynamic light scattering measurement demonstrated that allyloxy nonyl-phenoxypropanolpolyoxyethyleneetherammonium sulfonate (ANPS) was suitable for phthalocyanine blue pigment modification. The polymer-encapsulated phthalocyanine blue pigment dispersion with the small particles was obtained when the mass ratio of ANPS to phthalocyanine blue pigment, styrene (St) to phthalocyanine blue pigment, and ammonium persulfate (APS) to St was about 0.2, 0.2, and 0.01, respectively. Transmission electron microscopy (TEM), Fourier transforms infrared spectra (FTIR) and thermogravimetric analyses (TGA) provided supporting evidences for the encapsulation of phthalocyanine blue pigment with the formed copolymer. The polymer-encapsulated phthalocyanine blue pigment dispersion showed excellent stabilities to freeze–thaw treatment and centrifugal force.     

Dense Bi3Fe0.5Nb1.5O9 ceramics prepared by spark plasma sintering

Bi₃Fe_0.5Nb_1.5O₉ ceramics have attracted much attention due to its interesting dielectric and magnetic properties. However, the Bi₃Fe_0.5Nb_1.5O₉ ceramics prepared by the conventional solid state reaction method have a maximum density of about 60% of the theoretical density. Decomposition at temperatures higher than 850 °C precluded the preparation of a more highly dense sample. In the present research, dense ferroelectric Bi₃Fe_0.5Nb_1.5O₉ ceramics with a density of more than 97% of the theoretical one were prepared by spark plasma sintering. XRD data shows that Bi₃Fe_0.5Nb_1.5O₉ has an orthorhombic Aurivillius-type structure.     

Simultaneous improvement of thermal conductivity and mechanical properties for mechanically mixed ABS/h-BN composites by using small amounts of hyperbranched polymer additives

Recently, thermal interface materials (TIMs) are in great demands for modern electronics. For mechanically mixed polymer composite TIMs, the thermal conductivity and the mechanical properties are generally lower than expected values due to the sharply increased viscosity and poor filler dispersion. This work shows that addition of a small amount of polyester-based hyperbranched polymer (HBP) avoided the trade-off in mechanically mixed ABS/hexagonal boron nitride (h-BN) composites. After adding 0.5 wt% HBP, the maximum h-BN content in the composites increased from 50 to 60 wt%. The out-of-plane, in-plane thermal conductivity, and tensile strength of ABS/h-BN with 50 wt% h-BN were 0.408, 0.517 W/mK, and 18 MPa, respectively, and were increased to 0.729, 0.847 W/mK, and 32 MPa by adding 0.5 wt% HBP, while 0.972, 1.12 W/mK, and 29.5 MPa were achieved for ABS/h-BN/HBP with 60 wt% h-BN. The morphological and rheological results proved that these enhancements are due to the improved h-BN dispersion by decreasing viscosity of composites during mixing. Theoretical modeling based on the modified effective medium theory confirmed such results and showed that the interfacial thermal resistance also decreased slightly. Thus, this work demonstrates a facile and scalable method for simultaneously improving the thermal conductivity and mechanical properties of thermoplastic-based TIMs.     

2020年国内外宏观经济形势分析及预判

2020年,预计全球贸易进展局势出现缓和,世界经济增长小幅回升至2.6%左右,主要经济体面临的贸易政策、货币政策和地缘政治局势等不确定性因素仍较多,世界经济增长面临的下行风险仍较大。2019年中国经济总体平稳,GDP增长6.1%。2020年我国经济将继续保持增长稳健、结构优化、动能转换的发展态势,预计将实现6.0%的增长。     

Tertiary‐amine‐free,non‐planar,sulfone‐containing,tetrafunctional epoxy and its application as a high temperature matrix

Non‐amine‐derived tetrafunctional epoxies have several advantages over the amine‐derived N,N,N′,N′‐tetraglycidyl‐4,4′‐diaminodiphenyl methane (TGDDM) in high temperature applications. Although two non‐amine‐derived tetrafunctional epoxies were developed in our laboratory, further improvements in toughness using less loading amount is still desirable. Thus, a tertiary‐amine‐free, non‐planar and triphenylmethane‐containing tetrafunctional epoxy (STFE) with a sulfone spacer was synthesized. When it was mixed with diglycidyl ether of bisphenol A (DGEBA) and cured with 4,4′‐diaminodiphenylsulfone (DDS), both thermal and mechanical performances outperformed TGDDM. Moreover, STFE modified system shows the highest toughness (35.7 kJ m^–2) among three amine‐free and triphenylmethane‐containing epoxies at merely 5 wt% loading. Molecular simulation and thermomechanical analysis results suggest that the improved mechanical properties could be related to the geometry of the molecule and larger free volume. Despite a marginal drop in T_g, the thermal degradation temperature is better than that of TGDDM/DDS. In addition, the moisture resistance of STFE/DGEBA/DDS is much better than that of TGDDM/DDS. Thus, STFE modified DGEBA could be a potential replacement for TGDDM in some high temperature applications. © 2020 Society of Chemical Industry     

注塑机料筒温度调控和计算机仿真研究

利用模糊控制和比例积分微分(PID)控制相结合的手段对注塑机料筒温度进行了控制,同时以Matlab 6.0软件为仿真平台,对料筒温度控制进行了模拟仿真研究。实验发现,在注塑机料筒升温过程中利用CHR整定的PID控制手段和模糊控制手段,恒温过程中利用人工整定的PID控制手段,可保证快速的料筒升温响应速率和稳定的保温过程。通过实际注塑实验对该仿真结果进行了验证,在十组实验中,料筒温度误差不超过2%,产品翘曲变形量不超过0.059 mm。     

Molecular Dynamic Simulation Insights into the Normal State and Restoration of p53 Function

As a tumor suppressor protein, p53 plays a crucial role in the cell cycle and in cancer prevention. Almost 50 percent of all human malignant tumors are closely related to a deletion or mutation in p53. The activity of p53 is inhibited by over-active celluar antagonists, especially by the over-expression of the negative regulators MDM2 and MDMX. Protein-protein interactions, or post-translational modifications of the C-terminal negative regulatory domain of p53, also regulate its tumor suppressor activity. Restoration of p53 function through peptide and small molecular inhibitors has become a promising strategy for novel anti-cancer drug design and development. Molecular dynamics simulations have been extensively applied to investigate the conformation changes of p53 induced by protein-protein interactions and protein-ligand interactions, including peptide and small molecular inhibitors. This review focuses on the latest MD simulation research, to provide an overview of the current understanding of interactions between p53 and its partners at an atomic level.