Study on Interfacial Interlocking Effect of Ultrasonic Vibration-Assisted Adhesive Bonding.

Carbon fiber reinforced polymer (CFRP) blades are often exposed to wild and even harsh environments. The durability of the blade can be greatly improved by adhesively bonding a Ni erosion shield to the leading edge. In a traditional bonding process, the permeation of adhesive is poor at the interface, which gives an insufficient micromechanical interlocking. In this study, ultrasonic vibration was applied during the bonding process of sandblasted Ni plates and CFRP laminates. The values of shear strength were measured by tensile tests to verify the strengthening effect of applying ultrasonication. The cross-section of the bonded interface was characterized by scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS), and the surfaces with different treatments were explored by atomic force microscopy (AFM). The cross-sectional morphology and failure model of the samples were investigated. The strengthening mechanism was then studied by a molecular dynamics method. For the simulation of molecular dynamics, the CFRP/Ni bonding interface model was designed using the Materials Studio software package. The Perl scripts were used to simulate the ultrasonic vibration with different frequencies and amplitudes. The results showed that the ultrasonic process could improve the permeability and uniformity of the adhesive, enhancing the micromechanical interlocking effect.

Photochromism of novel molybdate/alkylamine composite thin films.

Novel inorganic/organic composite films of molybdates with photochromic properties have been prepared by self-assembly using alkylammonium ions as a supramolecular template. Both 1-hexadecylammonium/polyoxomolybdate (C16-Mo) and 1-octadecylammonium/polyoxomolybdate (C18-Mo) composite films have been successfully fabricated. The elemental analysis and thermal gravimetric analysis show that the main product in the C16-Mo film was (C16H33NH3)4Mo8O26. The X-ray diffraction (XRD) results indicate that the composite films were lamellar in nature. The IR, Raman and X-ray photoelectron spectroscopy (XPS) results show that the polyoxomolybdate anions present as MoO6 octahedra and that the Mo species exists as Mo6+ in the freshly prepared films. The alkyl chains in the 1-hexadecylammonium chains were linear and the alkyl groups are an all-trans configuration. Upon UV irradiation of the C16-Mo films, some Mo6+ was reduced to Mo5+, some -NH3+ became -NH2 with a concomitant increase in the concentration of -OH groups on the molybdate moieties, and the films were colored. Thus, the photochromism of the films involves the reduction of Mo6+ to Mo5+, coupled with a proton transfer from 1-hexadecylammonium ions to an oxygen atom at the Mo site. In contrast to thin films of transition-metal oxides, which all show photochromism in the blue region of the electromagnetic spectrum, these composite films show photochromism in the violet region with the greatest absorbance change at 472 nm.

Nanoparticles with Raman spectroscopic fingerprints for DNA and RNA detection.

Multiplexed detection of oligonucleotide targets has been performed with gold nanoparticle probes labeled with oligonucleotides and Raman-active dyes. The gold nanoparticles facilitate the formation of a silver coating that acts as a surface-enhanced Raman scattering promoter for the dye-labeled particles that have been captured by target molecules and an underlying chip in microarray format. The strategy provides the high-sensitivity and high-selectivity attributes of gray-scale scanometric detection but adds multiplexing and ratioing capabilities because a very large number of probes can be designed based on the concept of using a Raman tag as a narrow-band spectroscopic fingerprint. Six dissimilar DNA targets with six Raman-labeled nanoparticle probes were distinguished, as well as two RNA targets with single nucleotide polymorphisms. The current unoptimized detection limit of this method is 20 femtomolar.