Lacquer sap has received much attention as a traditional natural resin because it is a renewable and eco-friendly biopolymer resource unlike artificial coating materials. However, strict drying conditions and long drying times of lacquer sap should be modified to expand its applications. This study presents the first attempt to investigate the effect of different amplitudes of ultrasonic waves on the lacquer sap composed of water-in-oil (W/O) emulsion droplets and the mechanical properties of the resultant film by solvent evaporation. Acoustically induced cavitation via batch ultrasonication facilitates the generation of submicron-sized W/O emulsion. The drying time of sonicated lacquer sap was noticeably shortened as the amplitude of acoustic power increased. Interestingly, the transparency of the film cast from lacquer sap consisting of the smallest emulsion droplets increased significantly, weakening the degree of colour change from caramel-like yellow to dark brown as polymerisation progressed. These are attributed to the effective and frequent contact of laccase enzyme with urushiol at the increased interfacial area of nano-emulsified W/O droplets pulverised by ultrasonic waves. The quinone radical-generation in the interface layer and its transfer to the urushiol oil phase through water-insoluble glycoprotein emulsifier are greatly promoted, resulting in highly cross-linked, dense three-dimensional polymer networks, which also increased the lacquer film hardness after drying. As the emulsion droplet size decreased, the mutual interaction between the catechol moiety of urushiol and the substrates increased, resulting in improved adhesion. The nano-emulsification of the lacquer sap by ultrasonic waves can be used in a simple, effective, and eco-friendly way to shorten the drying time and improve the film characteristics of natural resins. This approach could pave the way for its wide range of applications in industrial fields, taking into account green and sustainable chemistry. 相似文献
In this paper, molecular dynamics tensile simulations of an amorphous polyethylene/graphene (PE/G) interface are carried out to investigate its adhesion strength. The effect of PE chain length and number and functionalization of G surface on the tensile behavior and interfacial adhesion is studied. The results show that the adhesion strength enhances with increasing chain length and number of the PE chains. In addition, the functionalization of G surface causes an increase in the adhesion strength comparing to unfunctionalized G due to deformation of a larger volume of the PE chains relying on the functionalized G. The contribution of bond length, bond angle, torsional potentials, and nonbonded energy is estimated as a function of interface elongation to clarify the deformation mechanisms within different tensile regions. The energy partitioning results indicate that the elastic, yield, and early postyielding regions are mostly controlled by the nonbonded interactions. However, the dihedral motions of the chains in addition to nonbonded interactions show a significant role in the disentanglement region, a part of postyielding and separation region. Furthermore, the simulation results exhibit how the internal mechanism associated with density profile, chain entanglements, and ordering can be evolved with increasing the interface elongation.
We study a dynamic interfacial slip phenomenon in filled polymer melts. When a poly(dimethyl siloxane) melt of weight average molecular weight Mw = 93 700 is mixed with glass beads of diameter up to 45 m, the sample shows some evidence of breakdown of interfacial adhesion between the glass beads and the PDMS matrix at a level of oscillatory stress under which the pure PDMS melt exhibits no decay. The decay of viscoelastic properties with time is essentially independent of the amplitude of shear strain as long as the magnitude of the oscillating stress is sufficiently high. It is suggested that much higher local stress than the apparent applied stress may be generated between the narrowly spaced beads. The interfacial slip was observable because it was measured against a natural length scale d in the filled polymer melts which is the filler size or the inter-filler distance and is much smaller than the dimensions of the flow cell. The decay under high stress and healing of interfacial adhesion upon a large reduction in stress may be related to the de-bonding and reformation of hydrogen bonds between the PDMS chains and the glass bead surfaces. 相似文献
A damage accumulation model for shear fatigue of asphalt-stone adhesion was developed with the aid of experimental data obtained from monotonic and dynamic force-controlled tests. Constant static- and stress-rate monotonic tests and cyclic fatigue tests were performed on the special designed specimens of double-layered-sandwich using dynamic thermal mechanics analyzer. Experimental results showed that it was feasible to describe monotonic and cyclic tests of stress-controlled mode using one single damage accumulation model based on stress–time path, which makes it possible to reduce the number of specimens tested and time-consuming fatigue tests are no longer necessary, since the same information can be obtained from monotonic test data without loss of accuracy. It also found that the bonding fracture in shear mainly attributes to cohesive failure through binder interlayer due to extensive creep deformation. 相似文献
A switchable dry adhesive based on a nickel–titanium (NiTi) shape‐memory alloy with an adhesive silicone rubber surface has been developed. Although several studies investigate micropatterned, bioinspired adhesive surfaces, very few focus on reversible adhesion. The system here is based on the indentation‐induced two‐way shape‐memory effect in NiTi alloys. NiTi is trained by mechanical deformation through indentation and grinding to elicit a temperature‐induced switchable topography with protrusions at high temperature and a flat surface at low temperature. The trained surfaces are coated with either a smooth or a patterned adhesive polydimethylsiloxane (PDMS) layer, resulting in a temperature‐induced switchable surface, used for dry adhesion. Adhesion tests show that the temperature‐induced topographical change of the NiTi influences the adhesive performance of the hybrid system. For samples with a smooth PDMS layer the transition from flat to structured state reduces adhesion by 56%, and for samples with a micropatterned PDMS layer adhesion is switchable by nearly 100%. Both hybrid systems reveal strong reversibility related to the NiTi martensitic phase transformation, allowing repeated switching between an adhesive and a nonadhesive state. These effects have been discussed in terms of reversible changes in contact area and varying tilt angles of the pillars with respect to the substrate surface. 相似文献
A simple method is described for the patterned deposition of Teflon on paper to create an integrated platform for parallel organic synthesis and cell‐based assays. Solvent‐repelling barriers made of Teflon‐impregnated paper confine organic solvents to specific zones of the patterned array and allow for 96 parallel flow‐through syntheses on paper. The confinement and flow‐through mixing significantly improves the peptide yield and simplifies the automation of this synthesis. The synthesis of 100 peptides ranging from 7 to 14 amino acids in length gave over 60 % purity for the majority of the peptides (>95 % yield per coupling/deprotection cycle). The resulting peptide arrays were used in cell‐based screening to identify 14 potent bioactive peptides that support the adhesion or proliferation of breast cancer cells in a 3D environment. In the future, this technology could be used for the screening of more complex phenotypic responses, such as cell migration or differentiation. 相似文献
Dynamic materials have been widely studied for regulation of cell adhesion that is important to a variety of biological and biomedical applications. These materials can undergo changes mainly through one of the two mechanisms: ligand release in response to chemical, physical, or biological stimuli, and ligand burial in response to mechanical stretching or the change of electrical potential. This study demonstrates an encrypted ligand and a new hydrogel that are capable of inducing and inhibiting cell adhesion, which is controlled by molecular reconfiguration. The ligand initially exhibits an inert state; it can be reconfigured into active and inert states by using unblocking and recovering molecules in physiological conditions. Since molecular reconfiguration does not require the release of the ligand from the hydrogels, inhibiting and inducing cell adhesion on the hydrogels can be repeated for multiple cycles. 相似文献