1. Introduction
In recent years, microbubbles have been actively investigated in the fields of microelectronic mechanical systems (MEMS), fluid dynamics systems, fluid biology, etc., due to their advantages, such as larger specific surface areas, longer underwater existence times, higher interface potential, and stronger adsorption capacity [
1,
2]. Microbubbles also have further applications in terms of sterilizing ozone water, enriching the oxygen of water, and water purification technology. Microbubbles are
orders of magnitude smaller in diameter than millibubbles. The buoyancy force of a microbubble is comparatively small, which leads to a slow floating-up behavior, and the floating-up velocity is significantly slower than that of a millibubble [
3]. Because microbubbles have a relatively long duration of stay underwater and absorbent properties, the suspending pollutants can be absorbed efficiently. Microbubbles can increase the buoyancy force of the suspending pollutants, thus leading the suspending pollutants to rise to the surface, which ultimately results in separating the solid impurities from the liquid, reducing the friction coefficient of the solid–liquid interface, and sterilizing them in the water. Underwater microbubbles are of great research significance in the aspects of drug delivery, catalytic reaction, underwater resistance reduction, gas collection, and wastewater treatment. Nowadays, the transportation technology of microbubbles requires contact with the surface of the medium, and the transport on the surface of the medium depends on the Laplace gradient force [
4,
5,
6].
However, the drawback of the process is that the velocity is slow, so the interface between the bubbles and the medium is hard to detach; simultaneously, the contact medium surface is required to be superhydrophobic in the air, whereas it appears as a superaerophilic surface underwater, which indicates a great limitation for the medium carrier used to transport the microbubbles [
7]. In addition, the transportation technology of contacting the surface of the medium also has some drawbacks, such as the transport bubble is unable to be eliminated. N. O. Young proposed that the Marangoni effect indicates an asymmetric change in the surface tension gradient of a liquid bubble, which is caused by temperature and gradient [
8]. In this case, the transportation of the bubble is observed under the effect of a surface tension gradient. The principal method of forming a liquid phase temperature gradient is external heating, as the most common heating mode is using Joule heat, which is generated by an electric field to form a temperature gradient [
9,
10,
11]. O. Zhoul et al. used Joule heat to realize the preparation of microbubbles in water [
12]. However, this method needs to solve problems such as circuit connections. Compared with electricity, light does not require wire integration, which is convenient and efficient, so the light source has become an ideal heating mode. There are few studies on the accumulation of heat by light-induced methods. However, carbon nanocoils have a favorable light absorption ability and thermal conductivity based on their unique morphology and structure [
13]. Our previous work has shown that carbon nanocoils as photothermal conversion materials are able to convert laser light energy into thermal energy, and the heat released during the process can be used to generate microbubbles in water.
In this study, we propose a new method for transporting microbubbles rapidly by a light-induced CNC immersed in water. The main purpose of a CNC as a laser irradiation carrier is to vaporize liquid around the position of the laser irradiation to allow the creation of microbubbles. It is evidenced that a light-induced CNC allows the creation of microbubbles at the start of the transport and the elimination of the microbubble at the end of the transport, which could provide new ideas for drug transport and water pollution treatment, etc.
2. Materials and Methods
The carbon nanocoils (CNCs) used in the experiment were prepared by chemical vapor deposition (CVD). A mixed solution of
9
O, and
O (with a concentration of
) is dropped on the quartz substrate as the catalyst precursor. After drying for 45 min, it is placed into the reaction furnace for calcination for 30 min (the calcination temperature is
) with argon as the shielding gas (the flow rate is 3
). After 30 min, acetylene and argon are introduced into the reaction furnace with a flow rate of
and
respectively, for 2 h (the reaction temperature is
) [
14]. Finally, CNCs with an average diameter of
and an average pitch of
were obtained. In order to obtain a single CNC in water, the CNCs
were peeled from the substrate and dispersed into deionized water
and a CNC aqueous solution was obtained after being ultrasonicated for 45 min. The length of the CNCs after ultrasonication is
µm to
µm. The CNC aqueous solution was injected into a polydimethylsiloxane (PDMS) microfluidic chip with microchannels (GH-LD-20, CChip scientific instrument Co., Ltd., Suzhou, China) at a flow rate of
by using a microsyringe pump (LSP01-2A, Longer Pump, Halma, Bucks, England) to form a liquid environment with the CNC attached to the bottom, as shown in
Figure 1a.
The laser optical system (optical tweezers system, LOT II, ZHONGKE Optical Tweezers Technology Co., LTD, Beijing, China) used in the experiment is shown in
Figure 1b. The wavelength of the laser light is
and can realize a continuously adjustable power output of
The beam diameter of the light source is
, which is enlarged to an
beam by the optical beam expander system, and finally focused by the focusing objective lens (
,
). The diameter of the focused spot is about
. The dynamics of the microbubble transport are recorded by a charge-coupled device (CCD) video system.
Figure 1c shows the schematic of the transport and elimination of the microbubble by the light-induced CNC. The microchannel with a rectangular cross-section is
in depth and
µm in width. The laser beam from the bottom to the top heats the CNC attached to the bottom of the microchannel. Then, the thermal energy is released into the water to vaporize the liquid around the light-induced site and form a temperature gradient in the water for transporting the microbubble. The bubble transport begins at the position where the bubble is created. The bubble can be eliminated at the end of the microbubble transport through mass and heat transfer.
To investigate the structural aspects of CNCs, the Raman spectra patterns of the samples were obtained by a Raman spectrometer under laser excitation and maximum output power of (Invia, Renishaw, Gloucestershire, England). The phase and crystal structures of the CNCs were studied by means of an X-ray diffractometer (XRD, Model - MiniFlex600, Rigaku, Tokyo, Japan).
3. Results
CNCs with an average diameter of 600 nm and an average pitch of
were obtained, as shown in
Figure 2a,b.
Figure 2c,d represent the X-ray diffraction (XRD) and the Raman spectrograms of the CNCs, respectively. The X-ray diffraction pattern of the CNCs exhibits two diffraction peaks at
and
, which are correlated to the (002) and (101) planes of the CNCs, respectively. The Raman spectrum of the CNCs comprises two prominent peaks at
and
, which correspond to the characteristics of the D and G bands of the carbon phase, respectively. Typically, D bands and G bands are associated with structural defects on the carbon basal plane and the sp2—hybridized graphitic structure of carbon materials, respectively.
Figure 3 shows that when the focused laser beam with a power of
irradiates the CNC in water, a microbubble with a diameter of 20 µm is formed instantaneously at the excitation point, and it is rapidly detached from the CNC surface to realize the radial free microbubble transport in water; the transport distance is
Ma et al. reported that CNCs have at least four pairs of energy bands that exist around the Fermi energy level, which are of benefit to the absorption of wavelengths in the NIR region [
15,
16]. Wang et al. studied the absorption spectra and the photoluminescence spectra of CNCs and found strong absorption bands in the NIR region and significant PL emissions in the NIR region [
13,
17], which indicate a CNC can convert laser photon energy into thermal energy efficiently, consequently increasing the temperature of the CNC’s surface. When the temperature is higher than the saturation temperature, there is an excess temperature of
, leading to the bubble nuclei forming on the concave surface of the CNC. On the basis of the heat transfer theory, the cavity structure on the heating wall surface provides the necessary conditions for the formation of bubbles. The concave section of the CNC is analogous to the cavity structure on the surface of the heating wall, which is more conducive to the accumulation of heat. The distance between the two concave sections is merely a few hundred nanometers, so the adjacent bubble nuclei merge into a spherical bubble nucleus attached to the tip of the spiral cone of the CNC during the development of the bubble nuclei. Its schematic diagram is shown in
Figure 4.
It is also observed in the experiment that when the laser power is lower, it takes a longer time for the bubble to separate from the CNC, and the diameter of the separated bubble is larger. On the contrary, when the laser power is higher, the time required for the bubble to separate from the CNC is shorter, and the diameter of the bubble is smaller. According to the theory of mass transfer and heat transfer [
18], due to the surface tension, there must be a pressure difference inside and outside the bubble; moreover, the liquid outside the bubble is a superheated liquid [
19]. The excess temperature is
. In this experiment, a theoretical model is developed:
is the surface temperature of the CNC (the heating wall temperature), and
is the saturation temperature. According to the Clausius–Clapeyron equation [
18,
20], the relationship between the excess temperature and the bubble diameter is represented by:
where
is the surface tension,
is the density of the gas inside the bubble,
is the latent heat of vaporization, and
is the bubble radius. It can be seen from the formula that
is inversely proportional to
. Thus, the laser power is higher for more energy absorption and conversion on the CNC and for a higher temperature of the CNC surface, as well as a higher excess temperature,
, of the CNC; then, as a consequence, the radius of the generated bubble is smaller.
Figure 5a shows the dynamics of microbubble formation, detachment, and transportation in deionized water within 1 s (laser power is
). The bubble is transported in the direction of the yellow arrows. Taking the focus of the laser radiation as the circle center, the heat on the CNC is not only used to form bubbles, but, also, the excess heat will be conducted to the surrounding liquid, thus a Laplace gradient of temperature will be formed along the radial direction [
21,
22]. The merged bubbles will be driven under the actions of temperature gradient force, buoyancy force, surface tension, viscous force, inertial force, etc. [
23,
24,
25]. In order to simplify the analysis, considering the invalidation of gravity and buoyancy in the microgravity environment, and viscous force and inertial force are negligible, then the temperature gradient force is the main driving force for the bubbles, while the surface tension is the main resistance to the transportation. After the bubble nucleation (after
), the relationship between the transport distance and the transport duration is linear, as shown in
Figure 5b.
Additionally, the experiments found that continuous multi-bubbles can be formed from the CNC one by one, then detached and transported in a row along the radial direction. After the first bubble is formed, the second and third bubbles are formed successively, and the process of transport is completed, as shown in
Figure 6a. To obtain a smaller bubble, the laser power is adjusted. When the first smaller bubble accomplishes the entire circulation of forming, transporting, and disappearing, the identical circulation of formation, transport, and disappearance of the second bubble begins. Then, after an interval of 0.05 s, the circulation of the third bubble is activated, as shown in
Figure 6b. It takes 0.1 s for each bubble to complete its circulation. When the specific surface of the bubbles is relatively large, the mass transfer and heat transfer are slow; furthermore, it takes a longer time for the bubbles to shrink and disappear, which is slower than the formation time of new bubbles. Thus, there is a phenomenon of continuous multiple bubbles transporting along the radial direction. When the size of the microbubbles is relatively small, the specific surface of the bubble is small, the mass and heat transfer is faster, and the time it takes for the bubbles to shrink before disappearing is shorter. The bubbles disappear before new bubbles are generated. Additionally, the transportation distance of small bubbles is shorter than that of large bubbles, due to the shorter existence time of small bubbles.
Since the focused laser has an optical trapping force on the CNC [
26,
27], the CNC will be far away from the focus position of the laser focus under the action of the optical trapping force and the thermal flow field, etc. Therefore, the action time for the laser and CNC is relatively short. The circulation of nucleation, growth, and detachment will be completed quickly under high-power laser irradiation. Large extrapolation pressure on the surrounding liquid during the rapid expansion of the bubbles accelerates the bubble separating from the CNC, which means no energy conversion is supplied by the CNCs for the growth of the bubble, and the liquid around the bubble cannot be vaporized into water vapor and enter the inside of the bubble through the boundary layer. The transfer of mass and heat in the boundary layer between the bubble and the liquid can be determined by two factors: one is the temperature difference between the liquid far away from the boundary layer and the water vapor inside the boundary layer, while the second is the pressure difference inside and outside the bubble. Temperature difference is the driving force for heat transfer, as the pressure difference is the driving force for mass transfer. As the heat transfer proceeds, the temperature and pressure inside the bubble gradually decrease, and the volume of the bubble gradually shrinks until it disappears. The relationship between the bubble diameter and the time of bubble shrinkage and disappearance is shown in
Figure 7. The shrinking velocity of the bubble is relatively slow in the initial stage, and it becomes faster and faster afterward, owing to the decrease in the bubble-specific surface area. The inset in
Figure 7 shows the process of shrinking and disappearing.
Figure 8 indicates that the laser beam irradiated on the bubble did not restrain the bubble from shrinking, and the bubble still continued shrinking until it disappeared. Compared to bubble shrinkage curves without laser irradiation, there is no obvious change in the velocity curve, which indicates that the microbubble transport is not affected by the light field. The image of the bubbles does not become blurred and enlarged, which suggests that the bubbles did not leave the focal plane, that is, the bubbles did not float up or sink down. It further indicates that the bubbles are not attracted or repelled by the optical trapping force. Light forces cannot drive the transport of bubbles. In the absence of the CNC as a heat-transfer carrier, the photon energy of the laser cannot be effectively converted into thermal energy inside and outside the bubble, or the light radiation energy is not enough to cause the gas–liquid phase transition, which in turn affects the growth and shrinkage of the bubble. The microbubble transport is not attributed to thermal convection caused by localized heating of the DI water by the laser, either. It can be seen from
Figure 8 that the shrinkage velocity of the bubbles under laser radiation does not decrease but increases slightly. This may be interpreted by the fact that when the laser irradiates microbubbles, with the generation of pressure [
23], the tangential thermocapillary force from the top to the bottom drives the liquid flow from the top of the bubbles to the bottom, and the liquid around the bubbles exerts pressure on the bubbles during this process, resulting in faster shrinking of the microbubbles.