Tribocorrosion Behavior of Micro/Nanoscale Surface Coatings.

Wear and corrosion are common issues of material degradation and failure in industrial appliances. Wear is a damaging process that can impact surface contacts and, more specifically, can cause the loss and distortion of material from a surface because of the contacting object's mechanical action via motion. More wear occurs during the process of corrosion, in which oxide particles or debris are released from the contacting material. These types of wear debris and accumulated oxide particles released during corrosion cause a combination of wear-corrosion processes. Bringing together the fields of tribology and corrosion research, tribocorrosion is a field of study which deals with mechanical and electrochemical interactions between bodies in motion. More specifically, it is the study of mechanisms caused by the combined effects of mechanical stress and chemical/electrochemical interactions with the environment. Tribocorrosion testing methods provide new opportunities for studying the electrochemical nature of corrosion combined with mechanical loading to establish a synergistic relationship between corrosion and wear. To improve tribological, mechanical, and anti-corrosion performances, several surface modification techniques are being applied to develop functional coatings with micro/nano features. This review of the literature explores recent and enlightening research into the tribocorrosive properties of micro/nano coatings. It also looks at recent discussions of the most common experimental methods and some newer, promising experimental methods in tribocorrosion to elucidate their applications in the field of micro/nano coatings.

Stages That Lead to Drop Depinning and Onset of Motion.

In this paper, we consider drops that are subjected to a gradually increasing lateral force and follow the stages of the motion of the drops. We show that the first time a drop slides as a whole is when the receding edge of the drop is pulled by the advancing edge (the advancing edge drags the receding edge). The generality of this phenomenon includes sessile and pendant drops and spans over various chemically and topographically different cases. Because this observation is true for both pendant and sessile cases, we exclude hydrostatic pressure as its reason. Instead, we explain it in terms of the wetting adaptation and interfacial modulus, that is, the difference in the energies of the solid interface at the advancing and receding edges. At the receding edge, a slight motion exposes to the air a recently wetted solid surface whose molecules had reoriented to the liquid and will take time to reorient back to the air. This results in a high surface energy at the solid-air interface which pulls on the triple line, that is, inhibits the motion of the receding edge. On the other hand, at the advancing edge, a slight advancement does not change the nature of the solid interfacial molecules outside the drop, and the advancing side's sliding can continue. Moreover, the solid molecules under the drop at the advancing edge take time to reorient, and hence, their configuration is not yet adapted for the liquid and therefore not adapted for retention of the advancing edge. Therefore, in sliding-drop experiments, the advancing edge moves before the receding one, typically a few times before the receding edge moves. For the same reason, the last motion of the receding edge usually happens as a result of the advancing edge pulling on it.

Comment on "Comparison of the Lateral Retention Forces on Sessile, Pendant, and Inverted Sessile Drops".

Tadmor et al.'s 2009 PRL article shows experiments of pendant drops with ∼30% higher retention forces than their sessile analogues. A recent article (de la Madrid, R. et al. Langmuir 2019, 35, 2871) seemingly explains this result theoretically using a drastically different experimental system that shows a ∼3% higher force that exceeds the scatter in three out of four data points. The differences between the two experimental systems might have allowed the two theories to coexist, but Tadmor's theory, which can explain both, allows an understanding of the solid-liquid interaction, which the newer theory lacks.

Droplets Sliding down a Vertical Surface under Increasing Horizontal Forces.

We have investigated the retention forces of liquid drops on rotating, vertical surfaces. We considered two scenarios: in one, a horizontal, centrifugal force pushes the drop toward the surface (?pushed drop? case), and in the other, a horizontal, centrifugal force pulls the drop away from the surface (?pulled drop? case). Both drops slide down as the centrifugal force increases, although one expects that the pushed drop should remain stuck to the surface. Even more surprising, when the centrifugal force is low, the pushed drop moves faster than the pulled drop, but when the centrifugal force is high, the pushed drop moves much slower than the pulled drop. We explain these results in terms of interfacial modulus between the drop and the surface.

Rapid Waterborne Pathogen Detection with Mobile Electronics.

Pathogen detection in water samples, without complex and time consuming procedures such as fluorescent-labeling or culture-based incubation, is essential to public safety. We propose an immunoagglutination-based protocol together with the microfluidic device to quantify pathogen levels directly from water samples. Utilizing ubiquitous complementary metal-oxide-semiconductor (CMOS) imagers from mobile electronics, a low-cost and one-step reaction detection protocol is developed to enable field detection for waterborne pathogens. 10 mL of pathogen-containing water samples was processed using the developed protocol including filtration enrichment, immune-reaction detection and imaging processing. The limit of detection of 10 E. coli O157:H7 cells/10 mL has been demonstrated within 10 min of turnaround time. The protocol can readily be integrated into a mobile electronics such as smartphones for rapid and reproducible field detection of waterborne pathogens.