火麻仁油微乳凝胶面膜的制备及初步评价

目的:制备火麻仁油微乳凝胶补水面膜并对其理化性质、保湿性和抗氧化活性进行评价.方法:通过伪三元相图确定火麻仁油微乳最佳处方,采用单因素及正交试验优化火麻仁油微乳凝胶处方,载入保湿活性物质制得火麻仁油微乳凝胶面膜并对其质量、稳定性、保湿性和抗氧化活性进行评价.结果:火麻仁油微乳最佳处方:火麻仁油0.2％、PEG-20氢化蓖麻油0.53％、1,3丙二醇0.27％.火麻仁油微乳凝胶最佳处方为卡波姆-940含量1％,丙三醇含量5％,稀释倍数30倍.制得的微乳凝胶澄清透明、涂展性较好、易清洗、不油腻;平均粒径为(30.91±0.31)nm,PDI为0.299±0.017,电位为(-3.54±0.43)mV;黏度为494725.15 mPa·s;pH值为5.50±0.01;保湿效果优于市售某凝胶面膜;火麻仁油微乳凝胶面膜对DPPH自由基清除率高于火麻仁油毛油,质量浓度为6 mg·mL-1时可达62.39％,IC50为3.71 mg·mL-1.结论:火麻仁油微乳凝胶面膜安全、稳定,制备工艺简单,对皮肤具有良好的补水和抗氧化效果,具备开发和推广的价值.     

Interfacial microstructure and mechanical properties of Ti3SiC2 ceramic and TC11 alloy joint diffusion bonded with a Cu interlayer

Reliable joints of Ti₃SiC₂ ceramic and TC11 alloy were diffusion bonded with a 50 μm thick Cu interlayer. The typical interfacial structure of the diffusion boned joint, which was dependent on the interdiffusion and chemical reactions between Al, Si and Ti atoms from the base materials and Cu interlayer, was TC11/α-Ti + β-Ti + Ti₂Cu + TiCu/Ti₅Si₄ + TiSiCu/Cu(s, s)/Ti₃SiC₂. The influence of bonding temperature and time on the interfacial structure and mechanical properties of Ti₃SiC₂/Cu/TC11 joint was analyzed. With the increase of bonding temperature and time, the joint shear strength was gradually increased due to enhanced atomic diffusion. However, the thickness of Ti₅Si₄ and TiSiCu layers with high microhardness increased for a long holding time, resulting in the reduction of bonding strength. The maximum shear strength of 251 ± 6 MPa was obtained for the joint diffusion bonded at 850 °C for 60 min, and fracture primarily occurred at the diffusion layer adjacent to the Ti₃SiC₂ substrate. This work provided an economical and convenient solution for broadening the engineering application of Ti₃SiC₂ ceramic.     

Controlled Secure Direct Communication Protocol via the Three-Qubit Partially Entangled Set of States

In this paper, we first re-examine the previous protocol of controlled quantum secure direct communication of Zhang et al.’s scheme, which was found insecure under two kinds of attacks, fake entangled particles attack and disentanglement attack. Then, by changing the party of the preparation of cluster states and using unitary operations, we present an improved protocol which can avoid these two kinds of attacks. Moreover, the protocol is proposed using the three-qubit partially entangled set of states. It is more efficient by only using three particles rather than four or even more to transmit one bit secret information. Given our using state is much easier to prepare for multiqubit states and our protocol needs less measurement resource, it makes this protocol more convenient from an applied point of view.     

柱塞卡滞原因分析

某柱塞泵工作中发生柱塞卡滞,经显微形貌观察、光谱分析、电子探针面扫描分析和显微硬度分析等,确定柱塞卡滞的根本原因为原材料组织中存在严重的网状共晶碳化物,降低了强度和韧性,增大了柱塞球面表层的脆性,进而导致了球面部位的接触疲劳抗力下降。严重的疲劳磨损与接触疲劳造成了柱塞球面脱层破坏,由此产生的金属碎屑进入柱塞与衬套的配合间隙处,进而限制了柱塞的自由运动。     

湖北省保康县荆山玉地球化学特征及其成因分析

荆山玉是湖北省保康县新发现的一个玉石品种,形成于大陆边缘—洋盆区过渡带的热水沉积环境,为晚震旦世—早寒武世灯影组的一种硅质角砾岩:原地震碎角砾岩,由角砾和胶结物二部分构成,角砾局部可拼接;角砾成分为早期硅质岩碎裂产物,胶结物除早期硅质岩碎裂产物外,还有少量后期充填的石英、铁质等,受角砾、胶结物颗粒大小、裂隙发育程度不同的影响,后期热液改造程度不同,角砾和胶结物化学成分存在一定的差异,色调与铁质有关。荆山玉的形成主要经历了三个阶段的演化:第一阶段,低温150～225℃、弱氧化—弱还原条件下热水成因的硅质岩形成;第二阶段,热力膨胀外力作用下,硅质岩局部原地震碎形成硅质角砾岩,热水温度243～340℃,富氧氧化—贫氧过渡环境,红褐色的Fe~(3+)在胶结物、裂隙中富集;第三阶段,热水温度116～127℃、缺氧还原条件,黄色的Fe~(2+)在胶结物、裂隙中富集。     

A facile method for preparation of PGS@ZB‐N and gas‐sol alternating synergistic effect for fire resistance of EVA

Through the simple precipitation of palygorskite (PGS) by zinc borate (ZB) (to make PGS@ZB) and the decoration of PGS@ZB by dodecylamine (N), a novel organic‐inorganic@inorganic hybrid flame retardant of PGS@ZB‐N was prepared and was incorporated with ethylene vinyl acetate copolymer (EVA) to improve its flame retardance. The structure and morphology of PGS@ZB‐N were characterized by Fourier transform infrared (FTIR) spectroscopy, X‐ray diffraction (XRD), and scanning electron microscopy (SEM), and it was confirmed that the PGS@ZB‐N hybrid had been successfully prepared. The flame retardancy and burning behavior of EVA/PGS@ZB‐N/EG (EG = expandable graphite) composite were studied through thermogravimetric analysis (TGA), limiting oxygen index (LOI), UL‐94 (by the vertical burning test), and cone calorimeter test (CCT) characterizations. The prepared EVA/PGS@ZB‐N/EG composite obtained an LOI value of 41.2% with the addition of 30 wt% PGS@ZB‐N/EG. It was found that EVA/PGS@ZB‐N/EG was protected through a gas phase and condensed phase alternating synergistic effect mechanism.