Clove essential oil emulsion-filled cellulose nanofiber hydrogel produced by high-intensity ultrasound technology for tissue engineering applications

High-intensity ultrasound (HIUS) was used to produce emulsion-filled cellulose nanofiber (CNF) hydrogel using clove essential oil (0.1, 0.5 and 1.0 wt%) as dispersed phase towards tissue engineering applications. The novel encapsulating systems obtained using HIUS specific energy at the levels of 0.10, 0.17, and 0.24 kJ/g were characterized by oil entrapment efficiency, microstructure, water retention value, color parameters, and viscoelastic properties. Freeze-dried emulsion-filled CNF hydrogels were characterized by porosity and swelling capacity. In addition, human gingival fibroblast cell cytocompatibility tests were performed to evaluate their potential applications as tissue engineering scaffold. The clove essential oil content strongly affected the oil entrapment efficiency, water retention value, color difference and whiteness of the prepared emulsion-filled CNF hydrogel. And, the HIUS energy only affected the yellowness of the emulsion-filled CNF hydrogel. Via HIUS processing, the CNF hydrogel successfully acted as a continuous phase in the emulsion-filled gel system with maximum oil entrapment efficiency of 34% when 0.5 wt% clove essential oil was added to the system. The encapsulating systems had predominantly gel-like property with maximum elastic modulus of 411 Pa. Furthermore, the emulsion-filled CNF hydrogels with the addition of clove essential oil up to 0.5 wt% indicated good cell viability rates (74–101%) to human gingival fibroblast cells. The newly developed clove essential oil emulsion-filled CNF hydrogel shows desirable cytocompatibility characteristics and can be considered as an alternative scaffold for tissue engineering applications.     

Spring-network model of red blood cell: From membrane mechanics to validation

Red blood cell membrane is highly elastic and proper modeling of this elasticity is essential for biomedical applications that involve computational experiments with blood flow. Inseparable and often some of the most difficult parts of modeling process are verification and validation. In this work, we present a revised model, which uses a spring network to represent the cell membrane immersed in a fluid and has been successfully used in blood flow simulations. We demonstrate the validation steps by first deriving the theoretical relations between the bulk properties of elastic membranes—shear modulus and area compressibility modulus—and parameters of the model that enter the nonlinear stretching and local area conservation computational moduli. We verify the theoretically derived relations using computer simulations of deformable triangular mesh. We calibrate the model by performing a computational version of the optical tweezers experiment. And finally, we validate the modeled cell behavior by investigating the cell rotation frequency when it is subjected to shear flow and cell deformation in narrow channels. The supplementary material contains an extensive dataset that can be used for setting different elastic properties for each cell in simulations of dense suspensions, while still conforming to the biological data. This work contains a complete model development process: From modelling of basic mechanical concepts (the spring network) and advanced biomechanical concepts (such as elasticity of the membrane), through calibration process towards the final stage of model validation.     

Effects of water freezing on the mechanical properties of nafion membranes

Most of the research efforts on Nafion have been devoted to the study of the perfluorinated ionomer membranes at optimal conditions for the desired applications, such as high temperature and low relative humidity for polymer electrolyte membrane fuel cells (PEM FC). In view of the possible changes induced by the freezing of water in the structure of Nafion and considering that in cold start conditions of a PEM FC device, Nafion needs to work also below 273 K, we measured the Young's modulus (Y) and the elastic energy dissipation (tan δ) in the temperature range between 90 and 470 K and the stress–strain curves between 300 and 173 K. The measurements reported here indicate that the mechanical properties of wet Nafion membrane change dramatically with temperature, that is, from a rubber‐like behavior at room temperature to a brittle behavior below 180 K. Moreover, we observed that the freezing of the nanoconfined water is complete only below 180 K, as indicated by a large increase of the Young's modulus. Between 180 and 300 K, the large values of tan δ suggest the occurrence of friction between the liquid water bound to the walls of the hydrophilic domains and the solid ice residing in the center of channels. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012     

Mesoscopic superelasticity,superplasticity,and superrigidity

Atomic-undercoordination-induced local bond contraction,bond strength gain,and the associated temperature （T）-dependent atomic-cohesive-energy and binding-energy-density are shown to originate intrinsically the exotic paradox of superplasticity,superelasticity,and superrigidity demonstrated by solid sizing from monatomic chain to mesoscopic grain.The paradox follows these relationships:（ε（K,T）y（K,T）σ（K,T））∝(exp(B/△T_mk),(η₁△T_mk)d～（-3）,[1+AK～（-2/2）exp(△T_mk/T)]△T_mkd～（-3）),（Plastic strain）（Elastic modulus）（Yield stress,IHPR）where A,B,η1,d and△T_mk=Tm（K） Tare size （K）-dependent physical parameters.Tm （K） is the melting point.Mechanical work hardening during compressing and self-heating during stretching modulate the measured outcome extrinsically.Superplasticity dominates in the solid-quasimolten-liquid transition state.The competition between the accumulation and annihilation of dislocations activates the inverse Hall-Petch relationship.Therefore,it is essential for one to discriminate the intrinsic competition between the local bond energy density gain and the atomic cohesive energy loss from the extrinsic factors of pressure and temperature in dealing with atomistic mechano-thermo dynamics.     

Modeling the impact of microcracking on the thermoelasticity of porous and microcracked ceramics

The foundations of the Integrity Factor Model are laid down and the model is discussed. The calculation of the internal stresses in microcracked materials (as a function of temperature) is done on the basis of both the macroscopic dilation and the lattice expansion measured by diffraction. The derivation is made starting from first principles for a single crystal, and then extending the approach to polycrystals, including complex microstructures, such as those containing porosity, microcracks, and multiple phases. Focus is cast on the fundamentals of the relationship between material properties and microstructure of anisotropic crystals, and on the resulting macroscopic behavior. The model is validated against experimental data, with the examples of the microcracked β-eucryptite and porous microcracked aluminum titanate composite.     

表面活性剂对气-液界面纳米颗粒吸附规律的影响

通过测定及分析纳米颗粒和表面活性剂-纳米颗粒复配体系在自由吸附过程与动态收缩过程中表面张力的变化,总结了纳米颗粒在气-液界面的吸附排布规律以及表面活性剂对其吸附规律的影响.实验结果表明,自由吸附过程中,随矿化度增加、阳离子活性剂浓度增加,平衡表面张力降低,这与颗粒吸附密度增加及颗粒润湿性改变有关.浓度低于临界胶束浓度(CMC)时,阳离子活性剂体系与混合体系的表面张力差异证明了阳离子活性剂可以通过静电作用吸附于纳米颗粒表面,进而部分溶解于水相;而阴离子活性剂与纳米颗粒相互作用力较弱,对表面张力影响较小.纳米颗粒体系在液滴收缩过程中,表面张力从自由吸附平衡态进一步降低大约9 m N/m,说明自由吸附过程中纳米颗粒不能达到紧密排布;同时表面张力呈现为缓慢降低、快速降低和达到平衡三部分,表面压缩模量可达70 m N/m,满足了液膜Gibbs稳定准则,这将有助于提高泡沫或者乳液稳定性.纳米颗粒-表面活性剂体系在液滴收缩过程中表面张力降低值随活性剂浓度增加而减小;表面压缩模量由高到低依次为:纳米颗粒>阳离子活性剂-纳米颗粒>阴离子-纳米颗粒>表面活性剂.     

Rheology of particulate rafts,films, and foams

Liquid foam exhibits remarkable rheological behavior although it is made with simple fluids: it behaves similar to a solid at low shear stress but flows similar to a liquid above a critical shear stress. Such properties, which have been proved to be useful for many applications, are even enhanced by adding solid particles. Depending on their hydrophobicity and size, the particles can have different geometrical configurations at the mesoscopic scale, that is, at the air–liquid interfaces, in the films, or in the interstices between the bubbles. In this review, we present rheological studies performed on granular rafts and films, on spherical armored interfaces, on gas marbles, and on aqueous foams laden with hydrophilic grains.     

Extracting uncrosslinked material from low modulus sylgard 184 and the effect on mechanical properties

Commercial silicone elastomers are commonly used in soft materials research due to their easily tunable mechanical properties. However, conventional polydimethylsiloxane (PDMS) elastomers with moduli below ∼100 kPa contain uncrosslinked free molecules, which play a significant role in their behavior. To utilize these materials, it is important to quantify what role these free molecules play in the mechanical response before and after their removal. We present a simple and inexpensive extraction method that enables the removal of free molecules from a lightly crosslinked sheet of Sylgard 184, a commercially available PDMS elastomer. The materials can contain a majority of free molecules yet maintain a thin and flat geometry without fractures after extraction. Subsequently, we compare the modulus, maximum stretchability, and hysteresis behavior with mixing ratios ranging from 60:1 to 30:1, before and after extraction. We show that the modulus, maximum stretchability, and dissipation increase upon extraction. Moreover, our approach offers a route to prepare crosslinked silicone elastomers with a modulus as low as ∼20 kPa without free molecules from a commercially available kit. © 2020 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 343–351     

Quantitative mapping of elastic moduli at the nanoscale in phase separated polyurethanes by AFM

The micro phase separated nanoscale morphology of phase separated polyurethanes (PUs) was visualized by atomic force microscopy (AFM) height and phase imaging of smooth surfaces obtained by ultramicrotonomy. PUs were obtained from 4,4′-methylenbis (phenyl isocyanate) (MDI), 1,4-butanediol (BD) and poly(tetrahydrofurane) polyether polyol (PTHF). The segmented polyether PUs with varying stoichiometric ratio of the isocyanate and hydroxyl groups were prepared to investigate the effect of molar mass, as well as the type and number of end-groups on their morphology and mechanical performance.The PU samples studied show characteristic “fingerprint” AFM phase images. Novel dynamic imaging modes of AFM, including HarmoniX material mapping and Peak Force Tapping were used to assess the mechanical performance of phase separated polyurethanes quantitatively as a function of their molecular structure. The values of surface elastic moduli were determined with nanoscale resolution and were in excellent agreement for both AFM modes. While tensile testing provides a bulk average value for the elastic modulus of the elastomers, the novel AFM based elastic moduli mappings introduced enable the study of surface stiffness with nanoscale resolution in a quantitative way.