skip to main content


Title: Effect of processing conditions on the mechanical properties of bio-inspired mechanical gradient nanocmposites
Photo-induced thiol-ene crosslinking of allyl-functionalized cellulose nanocrystal (CNC)/polymer nanocomposites allows access to films that mimic the water-enhanced mechanical gradient characteristics of the squid beak. These films are prepared by mixing the functionalized CNCs and polymer in a solvent before solution casting and drying. The photocrosslinking agents are then imbibed into the film before UV exposure. Reported herein are studies aimed at better understanding the effect of the film preparation procedure, film thickness and the conditions under which the UV treatment is carried out. It was found that when the film is heated at a temperature higher than its glass transition temperature (Tg) during the UV irradiation step there is a greater enhancement in the mechanical properties of the films, presumably on account of more efficient crosslinking between the CNC fillers. Moreover, composite films that were compression molded (at 90°C) before the imbibing step displayed lower mechanical properties compared to the as-cast films, which is attributed to phase separation of the CNC fillers and polymer matrix during this additional processing step. Finally, the film thickness was also found to be a critical factor that affects the degree of crosslinking. For example, thinner films (50 µm) displayed a higher wet modulus ca. 130 MPa compared to ca. 80 MPa for the thicker films (150 µm). Understanding the processing conditions allows access to a larger range of mechanical properties which is important for the design of new bio-inspired mechanical gradient nanocomposites.  more » « less
Award ID(s):
1844463
NSF-PAR ID:
10097388
Author(s) / Creator(s):
; ;
Date Published:
Journal Name:
European Polymer Journal
Volume:
115
ISSN:
0014-3057
Page Range / eLocation ID:
107-114
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Stable poly(styrene-co-2-ethylhexyl acrylate) latex particles with diameter less than 600 nm were prepared by the miniemulsion polymerization of Pickering emulsions stabilized with hexyl-functionalized cellulose nanocrystals (CNC-hexyl-COOHs). Polymer nanocomposites were fabricated by casting of the CNC-stabilized latex particles, and the thermomechanical properties and microstructures of the films were studied and related to the type and amount of stabilizer as well as the processing conditions. Compared to the latex films stabilized with low-molecular-weight sodium dodecyl sulfate (SDS) surfactant, or using a combination of SDS and carboxylic acid CNC-COOHs, films stabilized solely with the alkyl-functionalized CNC-hexyl-COOHs showed much higher storage moduli in the rubbery regime and lower water uptake. Scanning electron microscopy (SEM) revealed a CNC network structure that is formed by excluded volume effects of the latex particles, which concentrates the CNC-hexyl-COOHs into the interstitial space during solvent evaporation. This effect results in the formation of a percolation network at a lower CNC concentration within the latex composite films. The network can be further reinforced by increasing the concentration of CNCs through an “ex situ” process where CNC-hexyl-COOH-stabilized latex particles were mixed with CNC-COOH aqueous dispersions before film casting. The ability to replace low-molecular-weight surfactants in water-based latexes with alkyl-functionalized CNCs that are not only biosourced but also act as reinforcing agents offers an opportunity to expand the property profile of a variety of commercial products such as paints, coatings, and adhesives. 
    more » « less
  2. null (Ed.)
    Alignment of highly anisotropic nanomaterials in a polymer matrix can yield nanocomposites with unique mechanical and transport properties. Conventional methods of nanocomposite film fabrication are not well-suited for manufacturing composites with very high concentrations of anisotropic nanomaterials, potentially limiting the widespread implementation of these useful structures. In this work, we present a scalable approach to fabricate polymer-infiltrated nanoplatelet films (PINFs) based on flow coating and capillary rise infiltration (CaRI) and study the processing–structure–property relationship of these PINFs. We show that films with high aspect ratio (AR) gibbsite (Al (OH) 3 ) nanoplatelets (NPTs) aligned parallel to the substrate can be prepared using a flow coating process. NPTs are highly aligned with a Herman's order parameter of 0.96 and a high packing fraction >80 vol%. Such packings show significantly higher fracture toughness compared to low AR nanoparticle (NP) packings. By depositing NPTs on a polymer film and subsequently annealing the bilayer above the glass transition temperature of the polymer, polymer infiltrates into the tortuous NPT packings though capillarity. We observe larger enhancement in the modulus, hardness and scratch resistance of NPT films upon polymer infiltration compared to NP packings. The excellent mechanical properties of such films benefit from both thermally promoted oxide bridge formation between NPTs as well as polymer infiltration increasing the strength of NPT contacts. Our approach is widely applicable to highly anisotropic nanomaterials and allows the generation of mechanically robust polymer nanocomposite films for a diverse set of applications. 
    more » « less
  3. Polyurethane and polyurea-based adhesives are widely used in various applications, from automotive to electronics and medical applications. The adhesive performance depends strongly on its composition, and developing the formulation–structure–property relationship is crucial to making better products. Here, we investigate the dependence of the linear viscoelastic properties of polyurea nanocomposites, with an IPDI-based polyurea (PUa) matrix and exfoliated graphene nanoplatelet (xGnP) fillers, on the hard-segment weight fraction (HSWF) and the xGnP loading. We characterize the material using scanning electron microscopy (SEM) and dynamic mechanical analysis (DMA). It is found that changing the HSWF leads to a significant variation in the stiffness of the material, from about 10 MPa for 20% HSWF to about 100 MPa for 30% HSWF and about 250 MPa for the 40% HSWF polymer (as measured by the tensile storage modulus at room temperature). The effect of the xGNP loading was significantly more limited and was generally within experimental error, except for the 20% HSWF material, where the xGNP addition led to about an 80% increase in stiffness. To correctly interpret the DMA results, we developed a new physics-based rheological model for the description of the storage and loss moduli. The model is based on the fractional calculus approach and successfully describes the material rheology in a broad range of temperatures (−70 °C–+70 °C) and frequencies (0.1–100 s−1), using only six physically meaningful fitting parameters for each material. The results provide guidance for the development of nanocomposite PUa-based materials.

     
    more » « less
  4. Abstract

    Waterborne pressure sensitive adhesives (PSAs) consisting of polymer microparticle emulsions (i.e. latex) are more commonly used in commercial applications than solvent‐borne alternatives, as the use of water as a suspension medium provides better consumer safety and reduces environmental impact. However, the lower mechanical performance of waterborne PSAs prevents their use in applications requiring permanent adhesion or strong bonding between substrates. This reduction in mechanical strength is often attributed to void spaces that form during water evaporation and coalescence of the latex particles, and thus a potential strategy to improve PSA strength would be to add filler materials to occupy these voids. Fundamental studies investigating how interfacial interactions between the latex and fillers affect the collective strength of the films would enable better design of adhesive compositions to tailor PSA mechanical properties. Here we report the use of polymer brush‐grafted nanoparticles (PGNPs) as a means of mechanically reinforcing the PSAs, and determine how different aspects of the particle and polymer brush designs enable this improvement in adhesive performance. The PGNPs investigated here are intentionally designed to phase segregate into the aqueous phase of the initial latex suspension, which allows them to both fill free pore volume and also form multivalent supramolecular interactions with the latex particles to form polymer bridges that improve the interconnectivity of the final film. These studies provide insight into potential design strategies for tuning PSA properties with PGNPs, and enable up to 32% improvements to the cohesive strength of the PSAs without the typical deterioration of adhesive strength observed in PSAs using non‐brush‐coated particle fillers.

     
    more » « less
  5. BAlN films were grown by flow-rate modulation epitaxy on AlN. Figure 1 shows x-ray diffraction (XRD) peaks of 3-µm AlN/(0001) sapphire template layer and 45-nm BAlN layer at 2θ angles of 36.146o and 36.481o, corresponding to c-lattice constants of 4.966 and 4.922Å, respectively. The BAlN XRD peak is very clear and distinct given the small thickness, indicating good wurtzite crystallinity. It is not possible to directly calculate the B content from XRD alone because of uncertainty of the lattice parameters and strain. However, based on the angular separation of the XRD peaks and c-lattice constant difference, the B content is estimated to be ~7% [ ], which is considerably higher than those of high-quality wurtzite BAlN layers reported before [ , , ]. To obtain the accurate B content, Rutherford backscattering spectrometry (RBS) measurements are being made. Figures 2(a)-(b) show a high-resolution cross-sectional transmission electron microscopy (TEM) image with a magnification of 150 kx taken at a-zone axis ([11-20] projection) and diffraction pattern after fast-Fourier transform (FFT). A sharp interface between the AlN and BAlN layers is observed. In addition, the BAlN film exhibits a highly ordered lattice throughout the entire 45nm thickness without the polycrystalline columnar structures found in previous reports [1, ]. The FFT image confirms a wurtzite structure oriented along c-axis. Figure 3 shows a 5×5 µm2 atomic force microscopy (AFM) image of BAlN layer surface. The root-mean-square (RMS) surface roughness is ~1.7nm. Surface macro-steps were found on the surface due to longer diffusion length of group-III atoms than the expected step terrace width. This indicates there is potential to lower the growth temperature to create smoother surfaces while maintaining crystallinity which has been observed for AlN [ ]. In summary, a high-quality wurtzite BAlN layer with relatively high B content ~7% was demonstrated by MOCVD. Refractive index will be measured to facilitate design of distributed Bragg reflector (DBR) for deep UV vertical-cavity surface-emitting laser (VCSEL). 
    more » « less