Nature inspired solid–liquid phase amphibious adhesive

Here we report a new class of bio-inspired solid–liquid adhesive, obtained by simple mechanical dispersion of PVDF (polyvinylidene fluoride) (solid spheres) into PDMS (polydimethylsiloxane) (liquid). The adhesive behavior arises from strong solid–liquid interactions. This is a chemical reaction free adhesive (no curing time) that can be repeatedly used and is capable of instantaneously joining a large number of diverse materials (metals, ceramic, and polymer) in air and underwater. The current work is a significant advance in the development of amphibious multifunctional adhesives and presents potential applications in a range of sealing applications, including medical ones

Structural Reinforcement through Liquid Encapsulation

The liquid inside a solid material is one of the most common composite materials in nature. The interface between solid–liquid plays an important role in unique deformation. Here, model systems of two polymers (polydimethylsiloxane–polyvinylidenefluoride) are used to make sphere of solid with liquid inside it

Underwater adhesive using solid–liquid polymer mixes

Instantaneous adhesion between different materials is a requirement for several applications ranging from electronics to biomedicine. Approaches such as surface patterning, chemical cross-linking, surface modification, and chemical synthesis have been adopted to generate temporary adhesion between various materials and surfaces. Because of the lack of curing times, temporary adhesives are instantaneous, a useful property for specific applications that need quick bonding. However, to this day, temporary adhesives have been mainly demonstrated under dry conditions and do not work well in submerged or humid environments. Furthermore, most rely on chemical bonds resulting from strong interactions with the substrate such as acrylate based. This work demonstrates the synthesis of a universal amphibious adhesive solely by combining solid polytetrafluoroethylene (PTFE) and liquid polydimethylsiloxane (PDMS) polymers. While the dipole-dipole interactions are induced by a large electronegativity difference between fluorine atoms in PTFE and hydrogen atoms in PDMS, strong surface wetting allows the proposed adhesive to fully coat both substrates and PTFE particles, thereby maximizing the interfacial chemistry. The two-phase solid–liquid polymer system displays adhesive characteristics applicable both in air and water, and enables joining of a wide range of similar and dissimilar materials (glasses, metals, ceramics, papers, and biomaterials). The adhesive exhibits excellent mechanical properties for the joints between various surfaces as observed in lap shear testing, T-peel testing, and tensile testing. The proposed biocompatible adhesive can also be reused multiple times in different dry and wet environments. Additionally, we have developed a new reactive force field parameterization and used it in our molecular dynamics simulations to validate the adhesive nature of the mixed polymer system with different surfaces. This simple amphibious adhesive could meet the need for a universal glue that performs well with a number of materials for a wide range of conditions

Block Copolymer Elastomer with Graphite Filler: Effect of Processing Conditions and Silane Coupling Agent on the Composite Properties

The control of morphology and interface in poly(styrene-ethylene/butylene-styrene) (SEBS) composites with graphitic fillers is extremely important for the design of piezoresistive sensors for body motion or flexible temperature sensors. The effects of a high amount of graphite (G) and silane coupling agent on the morphology and properties of SEBS composites with anisotropic mechanical properties are reported. The physical and chemical bonding of silane to both G and SEBS surface was proved by EDX and TGA results; this improved interface influenced both the thermal and mechanical properties of the composite. The vinyltriethoxysilane (VS) promoted the formation of char residue and, being tightly bound to both SEBS and G, did not show separate decomposition peak in the TGA curve of composites. The mechanical properties were measured on two perpendicular directions and were improved by both the addition of VS and the increased amount of G; however, the increase of storage modulus due to orientation (from 5 to 15 times depending on the composition and direction of the test) was more important than that provided by the increase of G concentration, which was a maximum of four times that obtained for 15 wt % graphite. A mechanism to explain the influence of G content and treatment on the variation of storage modulus and tan δ depending on the direction of the test was also proposed

Raman Spectroscopy of Carbonaceous Materials: A Concise Review

A critical review focused on the Raman spectroscopy of carbonaceous materials and of polymer-based nanocomposites that contain carbonaceous (nano) materials as fillers is presented. The origin, assignment, and parameters (position, intensity, area, width, and shape) of main Raman modes (radial breathing mode, D-mode, G-mode, G\u27-mode, and so forth) as well as the effect of the interactions of carbonaceous materials on the parameters of these modes is briefly discussed. The effect of dopants and of polymeric matrices on the parameters of Raman bands is succinctly analyzed. The review will provide the basic and most elementary knowledge required to understand and discuss the Raman spectra of carbonaceous materials

Spectroscopic investigations on Polypropylene-Carbon Nanofiber Composites: I. Raman and Electron Spin Resonance Spectroscopy

Isotactic polypropylene-vapor grown carbon nanofiber composites containing various fractions of carbon nanofibers, ranging from 0 to 20 wt %, have been prepared. Raman spectroscopy was used to analyze the effect of the dispersion of carbon nanofibers within polypropylene and the interactions between carbon nanofibers and macromolecular chains. The as-recorded Raman spectra have been successfully fitted by a linear convolution of Lorentzian lines. Changes of the Raman lines parameters (position, intensity, width, and area) of polypropylene and carbon nanofibers were analyzed in detail. The Raman spectra of the polymeric matrix—at low concentrations of nanofibers—show important modifications that indicate strong interactions between carbon nanofibers and the polymeric matrix reflecting by vibrational dephasing of macromolecular chains. The Raman spectrum of carbon nanofibers is sensitive to the loading with carbon nanofibers, showing changes of the resonance frequencies, amplitudes, and width for both D- and G-bands. Raman data reveals the increase of the disorder, as the concentration of carbon nanofibers is increased. The presence of the typical ESR line assigned to conducting electrons delocalized over carbon nanofibers is confirmed and the presence of a spurious magnetic line due to catalyst’s residues is reported

Interface-Engineered Solid-Liquid Polymer Systems

This thesis explores the optimization and design of novel materials by engineering interfaces to impart novel mechanisms to polymer composites and multi-phase materials. By taking advantage of chemical and mechanical interactions it is possible to create materials with novel properties and unique mechanisms such as self-stiffening, self-healing, and adhesion. These properties arise due to large electronegativity differences which are repeated throughout the polymer chains which in turn give rise to strong macroscopic effects. The addition of a dynamic interface, an interface which can move and adapt under varying stress conditions, further enhances the unique properties of these materials. The composites discussed in this thesis were synthesized using a variety of techniques including thermal sonication/chemical synthesis, and mechanical synthesis. These novel composites were characterized using a myriad of techniques such as dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray computerized tomography (CT), in-situ scanning electron microscopy-based (SEM) mechanical testing, tensile testing (ADMET frame), SEM, transmission electron microscopy (TEM), contact angle (CA), optical microscopy, and qualitative testing

Fourier transform infrared spectroscopy and wide-angle X-ray scattering: Investigations on polypropylene–vapor-grown carbon nanofiber composites

Fourier transform infrared (FTIR) spectroscopy and wide-angle X-ray scattering (WAXS) investigations of isotactic polypropylene (iPP)–vapor-grown carbon nanofiber (VGCNF) composites containing various amounts of VGCNFs ranging between 0 and 20 wt %. are reported. The FTIR investigations were focused on the regularity bands of iPP. The FTIR data indicated a drop in the isotac­ticity index as the concentration of nanofibers was increased; this suggested a decrease in the crystallinity. WAXS measurements revealed a dominating α1 phase, with a small admixture of γ phase or mesophase. The loading of the polymeric matrix with car­bon nanofibers (CNFs) did not induce significant changes in the morphology of the polymeric matrix. A weak decrease in the size of α crystallites upon loading of CNFs was noticed. The experimental data obtained by FTIR spectroscopy supported the WAXS data. Spectroscopic data (a drop in the isotacticity index as estimated by FTIR spectroscopy and the ratio between the crystalline and total areas of WAXS lines assigned to iPP) failed to confirm the enhancement of the degree of crystallinity of polypropylene upon loading by nanofibers. However, whereas both techniques can identify with a high accuracy vibrations in ordered domains (FTIR spectroscopy) and the crystalline structure, including the lattice parameters and the size of crystallites (WAXS), difficulties in the correct assessment of the baseline and of amorphous components may result in important errors (typically \u3e5%) in the esti­mation of the degree of crystallinity of the polymeric component

Spectroscopic investigations on polypropylene-carbon nanofiber composites. I. Raman and electron spin resonance spectroscopy

Isotactic polypropylene-vapor grown carbon nanofiber composites containing various fractions of carbon nanofibers, ranging from 0 to 20 wt %, have been prepared. Raman spectroscopy was used to analyze the effect of the dispersion of carbon nanofibers within polypropylene and the interactions between carbon nanofibers and macromolecular chains. The as-recorded Raman spectra have been successfully fitted by a linear convolution of Lorentzian lines. Changes of the Raman lines parameters (position, intensity, width, and area) of polypropylene and carbon nanofibers were analyzed in detail. The Raman spectra of the polymeric matrix—at low concentrations of nanofibers—show important modifications that indicate strong interactions between carbon nanofibers and the polymeric matrix reflecting by vibrational dephasing of macromolecular chains. The Raman spectrum of carbon nanofibers is sensitive to the loading with carbon nanofibers, showing changes of the resonance frequencies, amplitudes, and width for both D- and G-bands. Raman data reveals the increase of the disorder, as the concentration of carbon nanofibers is increased. The presence of the typical ESR line assigned to conducting electrons delocalized over carbon nanofibers is confirmed and the presence of a spurious magnetic line due to catalyst\u27s residues is reported

Structural Reinforcement through Liquid Encapsulation

The liquid inside a solid material is one of the most common composite materials in nature. The interface between solid–liquid plays an important role in unique deformation. Here, model systems of two polymers (polydimethylsiloxane–polyvinylidenefluoride) are used to make sphere of solid with liquid inside it