Carbon nanotubes (CNTs) embedded polymers are of increasing interest to scientific and industrial communities for multi-functional applications. In this article, CNTs have been introduced to high-strength epoxy adhesive for enabling in-situ strain sensing in adhesively bonded aluminium-to-aluminium single-lap joints to accurately indicate the onset and propagation of adhesion failure to the evolution of piezo-resistivity in varying mechanical loads. The CNT modified adhesive in bonded joints and the CNT modified adhesive alone have been tested under monothonic and cyclic tensile loads up to ultimate failure. The changes in the piezo-resistivity induced by the CNTs have been monitored in situ with respect to loading. A novel interpretation method has been developed for progressive, instantaneous adhesion failure estimation under cyclic tensile stresses from a resistivity baseline. The method indicates that the in-situ resistivity changes and the rate of the changes with strain, i.e. sensitivity, strongly correlate with the adhesion failure progression, irrespective of the CNT dispersion quality. Moreover, the effect of bond thickness on the evolution of piezo-resistivity and adhesion failure have been studied. It was observed that relatively thin adhesive bonds (0.18 mm thickness), possessing higher CNT contact points than thick bonds (0.43 mm thickness), provide 100 times higher sensitivity to varying cyclic loads.
The pool-boiling performance of water on thin metal foils with graphene-oxide deposition was studied. The boiling performance was evaluated both on fully coated surfaces, achieved by spin-coating, and surfaces with a laser-textured nucleation site, into which graphene oxide was added via drop-casting. During the experiments, a high-speed IR camera was used to obtain the transient temperature and heat-flux distribution. At the same time, a high-speed video camera was used to acquire synchronized bubble-growth recordings. In addition, a surface-wettability analysis was conducted for all the samples. In the case of fully coated samples, graphene-oxide deposition resulted in an increased number of active nucleation sites and an increase in the nucleation temperature, leading to a lowered nucleation frequency. Meanwhile, samples with a single laser-textured nucleation site enabled the analysis of isolated vapor bubbles, confirming that graphene-oxide deposition leads to a higher nucleation temperature, consequently resulting in a larger bubble-departure diameter and longer growth time. Two explanations for the results are proposed: the wettability of graphene-oxide deposition and the filling of surface microcavities with graphene-oxide nanoflakes.
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