Flow-induced shear stress and deformation of a core–shell-structured microcapsule in a microchannel

A numerical model was developed and validated to investigate the fluid–structure interactions between fully developed pipe flow and core–shell-structured microcapsule in a microchannel. Different flow rates and microcapsule shell thicknesses were considered. A sixth-order rotational symmetric distribution of von Mises stress over the microcapsule shell can be observed on the microcapsule with a thinner shell configuration, especially at higher flow rate conditions. It is also observed that when being carried along in a fully developed pipe flow, the microcapsule with a thinner shell tends to accumulate stress at a higher rate compared to that with a thicker shell. In general, for the same microcapsule configuration, higher flow velocity would induce a higher stress level over the microcapsule shell. The deformation gradient was used to capture the microcapsule's deformation in the present study. The effect of Young's modulus on the microcapsule shell on the microcapsule deformation was investigated as well. Our findings will shed light on the understanding of the stability of core–shell-structured microcapsule when subjected to flow-induced shear stress in a microfluidic system, enabling a more exquisite control over the breakup dynamics of drug-loaded microcapsule for biomedical applications.     

Thermoset modified with polyethersulfone: Characterization and control of the morphology

Thermoset (TS) epoxy resins can be toughened with a thermoplastic (TP) for high-performance applications. The final structure morphology has to be controlled to achieve high mechanical properties and high impact resistance. Four polyethersulfone-modified epoxy resins are considered. They consist of different epoxy monomer structure (TGAP, triglycidyl-p-aminophenol and TGDDM, tetraglycidyl diaminodiphenylmethane) and a fixed amount of thermoplastic, and they are cured with two different amounts of curing agent. A reaction-induced phase separation occurs for all formulations generating morphologies, different in shapes and scales. The aim is to control the final morphology and in particular its dominant length scale. This morphology depends on the phase separation process, from the initiation to its final stage. The initiation relies on the relative miscibility of the components and on the stoichiometry between epoxy and curing agent. The kinetics depends on the viscosity of the systems. The different morphologies are characterized by electron microscopy or neutron scattering. Dynamic mechanical analysis allows confirming the presence of a phase separation even when it is not observable by electron microscopy. Vermicular morphologies with few hundreds nanometer width are obtained for the systems containing the TGAP as epoxy monomer. Systems formulated with TGDDM presents morphologies on much smaller scale of order a few tens of nanometers. We interpret the different sizes of the morphologies as a consequence of a larger viscosity for the TGDDM systems as compared to the TGAP ones rather than by a latter initiation of phase separation.     

Control of reaction mechanisms in cationically polymerized epoxy resins facilitates the adjustment of morphology and mechanical properties

Structure–property relations of cationically polymerized epoxy thermosets with different morphologies are examined. The morphology adjustment of amorphous epoxy based copolymers and partially crystalline polymer alloys is carried out with star‐shaped poly(ε‐caprolactone) (SPCL) bearing various numbers of hydroxyl end groups. These hydroxyl groups are known for their reactivity toward epoxides following the activated monomer (AM) mechanism. For this reason, four‐armed SPCL was synthesized with four hydroxyl end groups (SPCL‐tetraol) and, in addition, with successively esterified ones down to a SPCL with four ester end groups (SPCL‐tetraester). SPCL species bearing fewer or no hydroxyl end groups segregate into needle‐like nanodomains within the epoxy networks and, if the concentration is high enough, also into crystalline domains. The stronger phase separation of SPCL‐tetraester within the epoxy network compared with SPCL‐tetraol is due to a reduction of the AM mechanism. The mechanical properties resulting from different morphologies lead to a trade‐off between higher storage moduli and T_g values in the case of the more phase separated (and partially crystalline) polymer alloys and higher strain at break in the case of the amorphous copolymers. Nevertheless, in both cases toughness is improved or at least kept on the same level as for the pure epoxy resin. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 2188–2199     

海藻酸钠-壳聚糖-桑椹红微囊的制备

以海藻酸钠-壳聚糖为复合囊材采用锐孔法制备桑椹红微囊,探讨了海藻酸钠浓度、壳聚糖浓度、Ca Cl2浓度、桑椹红浓度、针头孔径、下滴高度、温度、转速等因素对微囊包封率的影响。确定了最佳制备工艺条件为海藻酸钠浓度4.0%、壳聚糖浓度2.5%、氯化钙浓度2.0%、桑椹红浓度0.50%、针头孔径0.390mm、下滴高度4cm、温度为20℃、转速为300r·min-1。制得的微囊药物含量为11.28%,包封率为88.93%。     

裂尖超钝化:实验、理论与数值模拟

本文报道了在改性聚丙烯裂尖平面应变段发生超钝化的实验发现。利用环向冷拉模型,可说明裂尖超钝化的形成取决于冷拉传播速率与加载率之比。裂尖超钝化可使材料韧性,尤其是冲击韧性的改善,达到一个新的水平。本文在超弹性-粘塑性各向异性损伤的有限变形本构模型下进行了详尽的数值计算。模拟结果成功地再现了裂尖超钝化的基本特征。     

CONTROL OF POLYMER PARTICLE SIZE USING POROUS GLASS MEMBRANE EMULSIFICATION A REVIEW

1.IntroductionPolymerparticleshavebeenusedinvariousfields.Besidestraditionalapplicationssuchaspaint,ink,andpaperindustries,muchattentionhasinrecentyearsbeenpaidtofineapplications,e.g.,carrierforenzyme(Omietal.,1997),separationmedia(Okubo&Hatorri,1993;Inomataetal.,1995;Ugelstadetal.,1992)forprotein,DNAandcell,andcarrierfordruginDrugDeliverySystem(DDS)(Paulettietal.,1997;Russell-Jones,2000).Controlofpolymerparticlesizeisespeciallyimportantinsuchfineapplications.Forexample,whenporouspartic…     

Ⅱ-Ⅲ混合型裂纹相变增韧分析

本文采用压力敏感准则和松函数法对相变增韧陶瓷Ⅱ-Ⅲ混合型裂纹的增韧效应进行了理论预测。分别给出了静止裂纹和定常扩展裂纹相变塑性屏蔽的理论表达式。结果表明：相变对静止裂纹有甚微的负屏蔽效应，并随KⅢ/KⅡ的比值而波动；相变对定常扩展裂纹的增韧结果除与材料弹性模量、相变尾区高度和相变体积分数有关外，还与KⅢ/KⅡ的比值有关。     

陶瓷阻力曲线测定的新方法——断裂栅法

将零厚度单向试件栅刻蚀工艺应用于晶须增韧氮化硅陶瓷基复合材料表面，通过记录试件所在桥路的输出电压值，可得到随载荷不断增大裂纹逐渐向前扩展过程中每一时刻的裂尖位置和裂纹长度，从而得到该种材料的阻力曲线。     

A NEW METHOD TO DETERMINE THE R-CURVE OF CERAMICS-FRACTURE GRATING METHOD

The etching technique of the single-lined zero-thickness specimen grating is applied tothe surface of the SiC fiber toughening Si_3N_4 ceramic composite specimen.The position of the crackand the crack length during the process of crack extension when the load is applied and gradually in-creased can be determined by recording the output voltage value of the Wheatstone bridge in which theceramic specimen with the fracture grating on is located.The crack-growth-resistance(R-curve) of thismaterialis thus obtained.