Abstract
Enrichment of colloidal particles in continuous flow has not only numerous applications but also poses a great challenge in controlling physical forces that are required for achieving particle enrichment. Here, we for the first time experimentally demonstrate the electrokinetically-driven continuous-flow enrichment of colloidal particles with Joule heating induced temperature gradient focusing (TGF) in a microfluidic convergent-divergent structure. We consider four mechanisms of particle transport, i.e., advection due to electroosmosis, electrophoresis, dielectrophoresis and, and further clarify their roles in the particle enrichment. It is experimentally determined and numerically verified that the particle thermophoresis plays dominant roles in enrichment of all particle sizes considered in this study and the combined effect of electroosmosis-induced advection and electrophoresis is mainly to transport particles to the zone of enrichment. Specifically, the enrichment of particles is achieved with combined DC and AC voltages rather than a sole DC or AC voltage. A numerical model is formulated with consideration of the abovementioned four mechanisms, and the model can rationalize the experimental observations. Particularly, our analysis of numerical and experimental results indicates that thermophoresis which is usually an overlooked mechanism of material transport is crucial for the successful electrokinetic enrichment of particles with Joule heating induced TGF.
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Introduction
Microfluidic technologies have been widely demonstrated with the potential of accurate and fast analyses/diagnoses in biological and chemical sciences as well as drug discovery1,2,3. Basically, microfluidics aims to integrate multiple steps of analyte manipulations in conventional analyses, usually consisting of sample concentration, pumping, mixing, chemical reactions, separation, detection and so on, into a single microchip. Therefore, microfluidics-based analytical devices gain various kinds of advantages over the conventional large-scale analytical systems, such as low analyte consumption and costs, fast analyses, good portability as well as high throughput etc. However, due to extremely small volumes of analytes (nanoliter or less) handled in microfluidic analyses, original low concentration of analytes would lead to poor detection which is a critical challenge faced by the microfluidics-based analytical systems4,5,6,7. To overcome this challenge has necessitated the pre-concentration of dilute samples prior to further manipulations, detection and analysis.
Generally, the methods for sample concentration can be divided into two large categories, non-electrokinetic methods and electrokinetic methods8. The popular non-electrokinetic methods include immunocapture based trapping9, magnetic beads assisted trapping10, thermophoretic trapping11 etc. Recently, there is also an emerging non-electrokinetic method which utilizes hydrodynamic inertia to enrich particulate analyte12,13,14. The electrokinetic methods also have been developed for analyte concentration in microfluidics. The advantages of electrokinetic methods include ease of control and applicability to a wide range of samples. One group of the electrokinetic concentrating techniques is the stacking method. In this technique, analytes migrate from one zone of higher velocity into another zone of lower velocity in which analytes become concentrated. The velocity change can be produced by two buffer solutions with different conductivities, such as field amplified sample stacking method15, 16 and isotachophoresis17,18,19. Although the concentration enhancement by the stacking method can be fairly high20, 21, it has several drawbacks, such as the need of multiple buffers, the requirement of relatively long channels, the limited concentration enhancement due to the insufficient difference between two buffer velocities, and the difficulty in controlling the concentrated samples because of their dynamic motion etc. Another group of electrokinetic analyte concentration technique is termed the field gradient focusing method, in which analytes are enriched at a unique equilibrium point where the net velocity of analytes is zero. The point of zero net velocity can be produced by pH gradient in the isoelectric focusing22, 23 or electric field gradient in the electric field gradient focusing24,25,26. The isoelectric focusing can achieve a relatively high concentration enhancement of 1000-fold as shown by both mass spectrometry analysis and direct imaging27. The isoelectric focusing however is limited to analytes with accessible isoelectric points. Electric field gradient focusing which manipulates the electric field in channels by patterning the shape and location of electrodes, usually involves complex design and tedious fabrication for electrodes. In addition to aforementioned two groups of electrokinetic methods, other electrokinetic concentration techniques in microfluidics include the trapping methods which make use of the concentration polarization near ion-selective membranes/nanofilters28,29,30,31,32, electrokinetic microvortices33, 34 and dielectrophoresis35, 36. Although the technique of ion-selective membranes can produce a concentration enhancement as high as million-fold29, it requires the sophisticated and expensive nanotechnology to fabricate nanochannels. The microvortices method involves the tedious surface treatment for modulation of surface charge or zeta potentials. The dielectrophoresis method produces limited concentration enrichment as well as requires sophisticated fabrication of complex electrode patterns.
Temperature gradient focusing (TGF) is a relatively new electrokinetic method for sample concentration in microfluidics. Essentially, TGF is one category of the field gradient focusing method. The point of zero velocity (focusing point) in TGF is produced by the velocity gradient due to the presence of a temperature gradient along the channel37. As compared to aforementioned concentration techniques, TGF can achieve the concentration of charged analytes in simple microfluidic structures with relatively short channel length38. The concept of TGF has been experimentally achieved for a variety of analytes, including amino acids, DNA and proteins and fluorescent dyes with temperature gradient produced by external heating/cooling equipment via electrical or optical means38,39,40. Usually, the application of electric field inevitably produces Joule heat in the conducting buffer solutions41. Then such Joule-heating method in combination with varying cross-section of channel provides an alternative way of setting up the temperature gradient required in TGF42,43,44. In comparison with the external heating mode, the Joule-heating mode does not require bulky external heating units, and thus consumes less power, simplifies the device design and fabrication, and enhances the portability and compactness of device. Recently, with a combined AC and DC electric field, an unprecedentedly high concentration enhancement of charged solute was accomplished with the Joule-heating mode of TGF45.
Noteworthily, Joule-heating mode of TGF so far has been only utilized for concentration of solutes. Practical applications frequently demand the concentration of particulate materials, such as the enrichment of bioparticles12, 46 for enhancing analysis sensitivity and the enrichment of colloidal particles34, 47 for colloid crystal assembly. Moreover, the existence of temperature gradient inevitably leads to thermophoresis which introduces another new mechanism of material transport neglected in the existing studies of TGF. In this paper, we report the electrokinetic enrichment of colloidal particles using Joule-heating induced TGF for the first time. We further demonstrate that dielectrophoresis and thermophoresis both play important roles in the enrichment of particles. Parametric studies under various experimental conditions (effects of electric field and particle size) are performed for examining the TGF performance. In addition, we formulate a multiphysical model to numerically simulate the experimental observations, and find that the modeling results can well account for the mechanisms of particle enrichment.
Results and Discussion
Effect of applied voltage on the particle enrichment
The images shown in Fig. 1 are the time evolution of enrichment of 1 µm particles dispersed in a 180 mM Tris-borate buffer under the effect of combined voltages of 700 V DC and 400 sin(2πft) V AC with f = 10 kHz. The contour images of measured fluorescent intensity in the left column indicate that the particles are enriched gradually near the narrowest constriction of the microfluidic channel. The images in the right column are the numerically simulated concentration of particles at four time instants corresponding to the experimental observations in the left column. Since the temperature gradient at the narrowest constriction of the channel is high so that the effect of thermophoresis of particles is expected, and a Soret coefficient of ST = −1.25 experimentally obtained for 1 µm particles was used in the numerical simulation48. Overall, the numerical model can reasonably describe the observed transient particle enrichment achieved by the Joule heating induced TGF. However, it should be noted that the numerical model fails to predict the deposition of particles on the walls near the constriction; this is because the numerical model presented in this study is for describing particle enrichment only, but not for describing particle deposition.
The particle enhancement can be characterized quantitatively by the particle concentration ratio which is defined as \(\bar{C}/{C}_{0}\) with \(\bar{C}\) being the averaged particle concentration across the narrowest constriction and C0 being the original particle concentration of testing samples. Figure 2 presents the concentration ratios of 1 µm particles at the narrowest constriction under three different cases of applied voltages. Our experiments find that for a fixed 400 V AC amplitude, there is a DC voltage window (from 600 V to 900 V) in which the enrichment of particles can be achieved and also becomes enhanced as the DC voltage increases (see the concentration enhancement from 700 V DC to 800 V DC in Fig. 2). No enrichment of particles occurs as the DC voltage falls outside of this window (either smaller than 600 V or larger than 900 V). For a fixed AC voltage, the DC voltage governs the following two effects: (i) The temperature and temperature gradient because of Joule heating, (ii) The particle transport by the combined action of electrophoresis and electroosmosis. Decrease of the DC voltage reduces the enrichment of particles because on the one hand the induced temperature gradient becomes smaller and thus suppresses the TGF, and on the other hand, less particles are transported to the constriction for enrichment. As the DC voltage drops below 600 V, effects of both (i) and (ii) are significantly reduced such that the particle enrichment vanishes. However, increase of the abovementioned two effects due to increasing DC voltage does not always contribute positively to the enrichment of particles. It should be noted that there is a competition between the abovementioned two effects as the DC voltage increases. Inside the DC window, an increase of effect (i) with the DC voltage dominates over that of effect (ii), leading to the enhancement of TGF and the associated particle enrichment; while further increasing the DC voltage above 900 V, the increment of effect (ii) predominates, and then particles move so fast through the constriction that the TGF is not strong enough to confine the particles to the constriction region.
Figure 2 also shows a nearly 200-fold concentration enhancement of particles within 100 s under a combined voltage of 800 V DC and 400 sin(2πft)V AC with f = 10 kHz. However, no particle enrichment was observed under sole applied DC electric voltage, even when the DC voltage was increased to 1100 V which generates much higher temperature and temperature gradient than the case of a combined voltage of 700 V DC and 400 sin(2πft)V AC with f = 10 kHz. Moreover, it was observed that under our experimental conditions all particles migrate from the left to the right, indicating that the electrophoretic motion of particles dominates over the TGF enrichment of particles. In order to achieve enrichment of particles, the DC electric field (associated with the electrophoretic velocity of particles) should be reduced while maintaining a sufficient temperature gradient for the TGF. Hence, with a combined AC and DC electric field, the AC component contributes to producing the temperature gradient via Joule-heating effect, and thus a lower DC voltage is preferred.
In addition, shown in Fig. 3 is the presence of a counterclockwise vortex near the constriction, and such vortex tends to dispel the enriched particles away from the constriction as the applied AC frequency is lowered to the order of 102 Hz. As discussed earlier, if the AC frequency is high (such as 10 kHz), the bulk flow is only due to the DC voltage driven electroosmosis. However, as the AC frequency decreases to the order of 102 Hz, the time period of AC electric field under such circumstance is comparable to the characteristic response time of the bulk electroosmosis flow in the microchannel (\({\tau }_{eof}=O({10}^{-2}){\rm{s}}\))49. Hence, such low frequency AC field allows the development of AC field driven electroosmosis, leading to the formation of vortical flows near the constriction as shown in Fig. 3 (see the corresponding movie in Supplementary Information). Furthermore, the electrothermal effect50, 51 could be another contributing factor to the formation of vortical flow in microfluidic constrictions. The experimental tests also indicate that the intensity of particle enrichment hardly changes when the AC frequency varies from 1 kHz to 100 kHz.
The role of thermophoresis in the enrichment of submicron particles
The strong variation of electric field in microfluidic convergent-divergent structure induces both dielectrophoresis and thermophoresis. Then a question naturally arises - which mechanism dominates the enrichment of small particles (such as 1 µm particles)? We carried out a controlled experiment to answer this question, and the experimental results are shown in Fig. 4. Since the conductivity of buffer solution is much larger than that of particles in present experiments, the dielectrophoretic force is independent of buffer concentration as suggested by Eq. (6) in Supplementary Information. Presumably, if the enrichment of 1 µm particles dispersed in the 180 mM Tris-borate buffer solution (Fig. 4(a) and its corresponding movie in Supplementary Information) is caused by dielectrophoretic trapping, the enrichment phenomena naturally should also be observable for particles dispersed in the Tris-borate buffer solution with a lower concentration. However, Fig. 4(b) amply shows no enrichment of particles in the 90 mM Tris-borate solution (see the corresponding movie in Supplementary Information). Hence, it is affirmative that the enrichment of smaller particles (1 µm particles) is not due to the dielectrophoresis. On the other hand, it should be noted that the reduction of buffer concentration (equivalent to the reduction of buffer conductivity) results in less Joule heat which could not sustain TGF of particles. So the absence of enrichment of particles in Fig. 4(b) verifies that the Joule-heating mode of TGF, instead of the dielectrophoresis, plays a dominant role in the concentration of 1 µm particles.
In order to clarify the role of thermophoresis in the enrichment of particles, the information of temperature field near the constriction is required. We thus measured the temperature distribution in the 180 mM Tris-borate buffer solution around the constriction region by using the Rhodamine B based thermometry whose principle is based on a sensitive temperature dependence of fluorescent intensity of Rhodamine B52. The general trend is that a decreasing Rhodamine B fluorescent intensity indicates an increasing solution temperature. In this experiment, the concentration of Rhodamine B in the solution was 0.1 mM, and the solution temperature was measured by using a calibrated relationship between temperature and fluorescent intensity reported previously48. Figure 5 shows the results of both temperature measurements and numerical predictions (note: the numerical model is presented in Supplementary Information). An inherent Joule heating induced temperature gradient is generated in the microchannel due to varying cross-sectional area of the channel. Expectedly, the temperature near the narrowest region of the channel is highest because of the largest electric current density, as is shown in Fig. 5(a) and (b). It is also noted that the variation of temperature mainly along the axial direction of the microchannel. Though there is temperature difference along the transversal direction of the channel, such difference is quite small because the channel is made from PDMS which has a much lower thermal conductivity than the buffer solution has. However, the temperature distribution around the constriction region is asymmetric which results from electroosmotic-flow-induced convective heat transfer from the right to the left. Figure 5(c) shows that despite certain difference between the numerical predictions and the experimental measurements, the numerical model can well capture the experimental trend. The deviation of the numerical model from the experiment could be due to some assumptions such as the uniform equivalent heat transfer coefficient and parameters such as zeta potential and other properties used in the numerical model as well as experimental errors. It is noted that the measured temperature gradient near the constriction is determined to be 1.5 × 105 K/m. Such a high temperature gradient usually gives to appreciable thermophoresis53, 54 which can play an important role in the TGF of particles.
To explore the detailed mechanisms of the particle enrichment in Joule heating induced TGF, we take advantages of the proposed numerical model to compute the profiles of axial velocities of 1 µm particles, induced by various mechanisms of particle transport along the centerline of the convergent-divergent structure, and the results are presented in Fig. 6. In the TGF, the particles are enriched at the location where the net velocity of particles becomes zero. Such zero net velocity of particles u net is predicted very near the constriction (see the solid dot in Fig. 6) and it leads to a continuous accumulation of the particles coming from both sides of the convergent-divergent channel. In other words, the zero-velocity point primarily determines the location of particle enrichment, and thus is also termed the point of enrichment. Furthermore, Fig. 6 shows that both the bulk electroosmosis and the electrophoresis (u + uep) transport the particles to the narrowest constriction where the thermophoretic velocity utp becomes significant to trap the particles. Here for 1μm particles the dielectrophoretic velocity udep plays an insignificant role; this is also in accord with the experimental observations in Fig. 4. In addition, for a comparison the figure also includes the profile of net velocity without inclusion of thermophoresis (see the dash line), and it is shown that the zero-velocity point or the enrichemet zone (see the hollow dot) shifts away from the narrowest constriction, which clearly differs from the experimental observation shown in Fig. 4(a).
Figure 6 already reveals an important role of the thermophoresis in determining the location of particle enrichment due to TGF. However, one still cannot figure out how thermophoresis would affect the particle enchantment quantitatively. As discussed early, the Joule heating induced TGF of 1 µm particles mainly results from several mechanisms (electroosmosis, electrophoresis and thermophoresis), and thus it is experimentally impossible to separate thermophoresis from other mechanisms because all mechanisms are highly coupled via temperature. Fortunately, the numerical simulation provides a way of identifying the effect of thermophoresis on particle enrichment by simply varying the magnitude of Soret coefficient. The simulation results of the concentration enhancement of 1 µm particles for three different strengths of thermophoretic effect are shown in Fig. 7. Our previous work showed that for the particles concentrated near the constriction, negative Soret coefficients (thermophilic behavior) are expected48. Figure 7(a) presents the concentration enhancement of particles after 150 s for ST = −1.25. The average concentration ratio of particles across the narrowest constriction is around 230, which is very close to the experimentally measured value of 219 in Fig. 2. Furthermore, the location and shape of the zone of particle enrichment are in reasonably good agreement with the experimental observations at 150 s shown in Fig. 1. As the magnitude of Soret coefficient decreases (say ST = −0.6 in Fig. 7(b)), the zone of particle enrichment shifts to the right side of the constriction, and the highest value of the concentration ratio is only about 5 which is significantly lower than the case when ST = −1.25. In absence of thermophoresis effect (say ST = 0 in Fig. 7(c)), the zone of particle enrichment moves further towards the right side of the constriction, and the concentration enhancement is further reduced. The numerical results in Fig. 7 adequately show that the thermophoresis attracts the particles from the low temperature region (the wide region) towards the higher temperature region (the narrow region), thereby leading to the particle enrichment at the constriction section.
Effect of particle size on the particle enrichment
Colloidal particles with three different diameters of 0.5 µm, 1 µm, and 5 µm were used in the experiments. The two smaller particles (0.5 µm and 1 µm) were successfully concentrated under a combined field of 700 V DC and 400 sin(2πft) V AC with f = 10 kHz. Figure 8 shows the variation of concentration ratios of 0.5 µm and 1 µm particles with time. It is seen that the concentration enhancement becomes stronger as the particle size increases from 0.5 µm to 1 µm. The magnitude of the Soret coefficient characterizing the strength of thermophoresis is smaller for 0.5 µm particles, as compared to that of 1 µm particles48. This suggests that 1 µm particles would acquire a higher velocity which facilitates the enrichment of particles.
However, with further increasing the particle size from 1 µm to 5 µm and under the same applied voltage, the trapped particles were observed to oscillate within the constriction region, as shown in Fig. 9(a). Here, we perform a qualitative analysis based on the preceding discussion of 1 µm particles to clarify the roles of dielectrophoresis and thermophoresis in the enrichment of 5 µm particles. The conclusions from several previous works48, 55, 56 suggested that the Soret coefficient of 5 µm particle is larger than that of 1 µm particle. However, the diffusivity of 5 µm particle is smaller than that of 1 µm particle by a factor of 5. According to Eq. (7) in Supplementary Information, one then expects that the thermophoretic velocity of 5 µm particle is comparable to that of 1 µm particle55. On the other hand, it is known that the dielectrophoretic force is scaled to the cubic power of particle size \((i.e.,\langle {\overrightarrow{F}}_{DEP}\rangle \propto {a}^{3})\) (see Eq. (6) in Supplementary Information). An increase of particle size from 1 µm to 5 µm would amplify the dielectrophoretic force 125 times. The resulting dielectrophoretic velocity of 5 µm particle then becomes 25 times of that of 1 µm particle (as shown by Eq. (5) in Supplementary Information). In other words, the dielectrophoretic velocity of 5 µm particle is enhanced by one order of magnitude as compared to 1 µm particle.
It is noted that from Fig. 6 that the thermophoretic velocity of 1 µm particle is nearly two orders of magnitude higher than its corresponding dielectrophoretic velocity. Considering this fact and the aforementioned discussion, we can conclude that the thermophoretic velocity of 5 µm particle is still at least one order of magnitude higher than its corresponding dielectrophoretic velocity. Consequently, the thermophoresis still plays a more important role than the dielectrophoresis in the enrichment of 5 µm particles. With further increment of the particle size, the dielectrophoresis would overtake the thermophoresis, and there would be eventually a transition from the thermophoresis-dominated enrichment to the dielectrophoresis-dominated enrichment. This is very different from the conventional conception that the enrichment of particles at microfluidic constrictions is only dominated by dielectrophoresis57, 58.
The oscillation of trapped 5 µm particles near the constriction is due to a force imbalance on particles induced by the predominant thermophoretic effect. Under the same AC electric field, as increasing the DC electric field from 700 V to 800 V, the enhancement of both the electrophoretic motion of particles (from the left to the right) and the thermophoretic trapping force on the particles can lead to the particle trapping on the right side of constriction as shown in Fig. 9(b). Two movies are submitted as the Supplementary Information for Fig. 9(a) and (b).
Conclusions
In this work, we have reported both experimental and numerical investigation of the enrichment of colloidal particles in a PDMS microchannel with a convergent-divergent structure. To our best knowledge, this is the first experiment demonstrating the particle enrichment with the Joule heating induced temperature gradient focusing method. In particular, the enrichment of colloidal particles was achieved by our proposed combined AC and DC field technique. Our experiments showed that the use of a combined AC and DC is superior to the use of a sole DC field. Furthermore, it was found that for a fixed AC voltage, there exists a window of applied DC voltages that can achieve successful particle enrichment. However, outside this DC voltage window, a lower DC voltage cannot produce sufficient Joule heating to induce temperature gradient required for enriching particles, and a higher DC voltage leads to fast motion of particles such that particles are swept away, with no enrichment at the constriction of the microchannel. In such case, a higher AC component is needed to produce a higher temperature gradient for TGF of particles.
Four modes of particle transport have been considered in the Joule heating induced TGF of particles, including advective motion of particles due to electroosmotic bulk flow, electrophoretic motion of particles, dielectrophoretic motion of particles and thermophoretic motion of particles. The experimental results suggest the electrokinetically driven TGF of particles is mainly ascribed to the thermophoresis for the particle size considered in this study. Due to the cubic power scaling of the force with particle size, the dielectrophoresis would dominate the particle enrichment as the particle size further increases beyond a critical value. The advection and electrophoresis of particles mainly contribute to transporting particles from the reservoirs to the zone of enrichment.
A numerical model is also formulated to describe the Joule heating induced TGF of particles under a combined AC and DC field. The numerical simulations can reproduce the experimental results reasonably well. Furthermore, the proposed numerical model allows gaining more physical insights into the observed particle enrichment by quantitatively providing the velocity profiles of the abovementioned four particle transport modes, which are apparently not accessible from the experiments. In addition, the numerical simulations verify that the existence of thermophoresis in the Joule heating induced TGF of relatively small particles not only enhances the particle enrichment but also helps to define the shape and location of the zone of particle enrichment.
Method
Equipment setup
The setup of entire experimental system is shown in Fig. 10. A fluorescence microscope (Carl Zeiss, Germany) equipped with a mercury lamp (mbq 52 ac, Zeiss) for excitation of fluorescent particles was used in the experimental investigation. The microfluidic device for concentrating microparticles consists of a straight PDMS channel with a convergent-divergent structure in the middle section of channel (see details in the top-left portion of Fig. 10). The PDMS channel with a length of 16mm, a height of 50 µm, a width of 1mm was fabricated using the standard soft lithography. The length of microfluidic convergent-divergent structure is 2mm, with the narrowest constriction being 100 µm. Two reservoirs with a diameter of 6mm were punched at the two ends of channel for introducing particle samples. Two platinum wires of 0.5 mm in diameter (Sigma-Aldrich, USA) placed in each reservoir were used for applying electrical voltages. To produce combined AC and DC voltages, the AC signal with DC bias was generated by a function generator (AFG3102 Dual Channel Arbitrary/Function Generator, Tektronix Inc.), and then was amplified to the required combined AC and DC voltage by a customized three-channel voltage amplifier (OPT3-AC800-DC1.5 K, Optrobio Technologies Pte Ltd). In order to maintain the accuracy of the input voltage to the microfluidic device, an oscilloscope (100 MHz CombiScope® HM1008-2, HAMEG Instruments) was used to monitor the voltage output from the amplifier. A power source (PS350, Stanford Research System, USA) was used for supplying pure DC voltages. The enriching phenomena were monitored through a 5x objective lens and then recorded with a CCD camera (Sensovation AG, Germany) at a rate of 15 frames per second.
The bottom-left portion of Fig. 10 presents the particle enrichment due to four transport mechanisms. As is shown, Joule heat generated in the conducting buffer couples with the varying channel cross-section to produce an axial temperature gradient. In the presence of electric field, electroosmotic flow of buffer solution is directed from the right to the left, dragging particle inside the solution to move with a velocity of u. The particle electrophoresis moves the particle from the left to the right with a velocity of uep, which is opposite to the electroosmotic bulk flow. The dielectrophoresis repels the particle from the region of high electric field strength towards the region of low electric field strength with a velocity of udep. The thermophoresis induces the motion of particle from the cold region to the hot region with a velocity of utp due to the strong temperature gradient produced by Joule heating. The imbalance of four particle transport mechanisms (u, uep, udep, utp) results in a net particle motion, and it directs particles to the constriction from both sides, thereby leading to the enrichment of particles at constriction.
Sample preparation
Green fluorescent particles of 500 nm, 1 µm and 5 µm (Thermo Fisher Scientific Inc.) were used in particle enrichment experiments. Because of the Thermo Fisher Scientific’s Firefli™ process, these florescent particles are highly stable and their fluorescence intensity is insensitive to the temperature change within the range of our experiment. Prior to the experiment, each original particle suspensions (1% w/w solids) were all diluted with a Tris-borate buffer solution (180 mM until specified otherwise) for 500 times volumetrically. Before being loaded into the microfluidic channel, all prepared colloidal samples were sonicated for 15 minutes in an ultrasonic cleaner (Elmasonic E30H, Elma Ultrasonics) for homogenization. Particularly, the Tris-borate buffer prepared from Tris(hydroxymethyl)aminomethane (Sigma-Aldrich, USA) and borate acid (Sigma-Aldrich, USA) was purposely used to maintain pH of the electrolyte medium.
Experimental procedure and image analysis
The microchannel with two reservoirs was first flushed with deionized water and then filled with the experimental sample solutions. After the electrodes were placed into the reservoirs, the buffer solution levels in two reservoirs were carefully adjusted for balance. This procedure ensures no induced flow by pressure difference resulting from the solution level difference in two reservoirs. Subsequently, the mercury arc lamp was turned on to illuminate the fluorescent particles. The power supply was then immediately switched on to generate electric field along the channel. At the same time, the grayscale fluorescent images were captured by the CCD camera and simultaneously recorded into a personal computer for subsequent analyses. In this study, two different modes of applied voltages, i) a combined AC and DC voltage, and ii) a sole DC voltage were tested as the applied electric field. For a combined AC with DC voltage, the AC component was fixed at 800 V (peak to peak voltage) which is the maximum AC voltage that can be supplied by our current voltage amplifier, and the DC bias was varied from 600 V to 900 V. For the case of sole DC voltages, it was varied from 700 V to 1100 V. For the sake of quantifying the enhancement of particle concentration, the grayscale value of microscopic images was extracted with a MATLAB program and subsequently converted to the concentration of particles by using the calibration curves provided in ref. 48.
References
Andersson, H. & van den Berg, A. Microfluidic devices for cellomics: a review. Sens. Actuators, B 92, 315–325, doi:10.1016/S0925-4005(03)00266-1 (2003).
Dittrich, P. S. & Manz, A. Lab-on-a-chip: microfluidics in drug discovery. Nat. Rev. Drug Discov. 5, 210–218, doi:10.1038/nrd1985 (2006).
Tu, Q. et al. Microfluidic Device: A Miniaturized Platform for Chemical Reactions. Chin. J. Chem. 31, 304–316, doi:10.1002/cjoc.201201212 (2013).
Verpoorte, E. Microfluidic chips for clinical and forensic analysis. Electrophoresis 23, 677–712, doi:10.1002/1522-2683(200203)23:5<677::AID-ELPS677>3.0.CO;2-8 (2002).
Scriba, G. K. E. Pharmaceutical and biomedical applications of chiral capillary electrophoresis and capillary electrochromatography: An update. Electrophoresis 24, 2409–2421, doi:10.1002/elps.200305491 (2003).
Crompton, T. R. Preconcentration Techniques for Natural and Treated Waters: High Sensitivity Determination of Organic and Organometallic Compounds, Cations and Anions. (Taylor & Francis, 2002).
Dittrich, P. S., Tachikawa, K. & Manz, A. Micro Total Analysis Systems. Latest Advancements and Trends. Anal. Chem. 78, 3887–3908, doi:10.1021/ac0605602 (2006).
Zhao, C., Ge, Z. & Yang, C. Microfluidic Techniques for Analytes Concentration. Micromachines 8, 28, doi:10.3390/mi8010028 (2017).
Kirby, B. J. et al. Functional Characterization of Circulating Tumor Cells with a Prostate-Cancer-Specific Microfluidic Device. PLOS ONE 7, e35976, doi:10.1371/journal.pone.0035976 (2012).
Talasaz, A. H. et al. Isolating highly enriched populations of circulating epithelial cells and other rare cells from blood using a magnetic sweeper device. Proc. Natl. Acad. Sci. 106, 3970–3975, doi:10.1073/pnas.0813188106 (2009).
Braun, D. & Libchaber, A. Trapping of DNA by Thermophoretic Depletion and Convection. Phys. Rev. Lett. 89, 188103, doi:10.1103/PhysRevLett.89.188103 (2002).
Martel, J. M. et al. Continuous Flow Microfluidic Bioparticle Concentrator. Sci. Rep. 5, 11300, doi:10.1038/srep11300 (2015).
Özbey, A., Karimzadehkhouei, M., Akgönül, S., Gozuacik, D. & Koşar, A. Inertial Focusing of Microparticles in Curvilinear Microchannels. Sci. Rep. 6, 38809, doi:10.1038/srep38809 (2016).
Go, T., Byeon, H. & Lee, S. J. Focusing and alignment of erythrocytes in a viscoelastic medium. Sci. Rep. 7, 41162, doi:10.1038/srep41162 (2017).
Burgi, D. S. & Chien, R. L. Optimization in sample stacking for high-performance capillary electrophoresis. Anal. Chem. 63, 2042–2047, doi:10.1021/ac00018a028 (1991).
Zhang, C.-X. & Thormann, W. Head-Column Field-Amplified Sample Stacking in Binary System Capillary Electrophoresis: A Robust Approach Providing over 1000-Fold Sensitivity Enhancement. Anal. Chem. 68, 2523–2532, doi:10.1021/ac951250e (1996).
Stegehuis, D. S., Irthu, H. & Tjaden, U. R. & Van Der Greef, J. Isotachophoresis as an on-line concentration pretreatment technique in capillary electrophoresis. J. Chromatogr. A 538, 393–402, doi:10.1016/S0021-9673(01)88860-9 (1991).
Gebauer, P. & Boček, P. Recent progress in capillary isotachophoresis. Electrophoresis 23, 3858–3864, doi:10.1002/elps.200290006 (2002).
Wang, J. et al. Online transient isotachophoresis concentration by the pseudo-terminating electrolyte buffer for the separation of DNA-aptamer and its thrombin complex in poly(methyl methacrylate) microchip. Analyst 136, 1142–1147, doi:10.1039/C0AN00434K (2011).
Jung, B., Bharadwaj, R. & Santiago, J. G. On-Chip Millionfold Sample Stacking Using Transient Isotachophoresis. Anal. Chem. 78, 2319–2327, doi:10.1021/ac051659w (2006).
Bottenus, D., Jubery, T. Z., Dutta, P. & Ivory, C. F. 10 000-fold concentration increase in proteins in a cascade microchip using anionic ITP by a 3-D numerical simulation with experimental results. Electrophoresis 32, 550–562, doi:10.1002/elps.201000510 (2011).
Righetti, P. G. & Bossi, A. Isoelectric focusing of proteins and peptides in gel slabs and in capillaries. Anal. Chim. Acta 372, 1–19, doi:10.1016/S0003-2670(98)00329-8 (1998).
Kohlheyer, D., Eijkel, J. C. T., Schlautmann, S., van den Berg, A. & Schasfoort, R. B. M. Microfluidic High-Resolution Free-Flow Isoelectric Focusing. Anal. Chem. 79, 8190–8198, doi:10.1021/ac071419b (2007).
Humble, P. H., Kelly, R. T., Woolley, A. T., Tolley, H. D. & Lee, M. L. Electric Field Gradient Focusing of Proteins Based on Shaped Ionically Conductive Acrylic Polymer. Anal. Chem. 76, 5641–5648, doi:10.1021/ac040055+ (2004).
Petsev, D. N., Lopez, G. P., Ivory, C. F. & Sibbett, S. S. Microchannel protein separation by electric field gradient focusing. Lab Chip 5, 587–597, doi:10.1039/B501538C (2005).
Hlushkou, D., Perdue, R. K., Dhopeshwarkar, R., Crooks, R. M. & Tallarek, U. Electric field gradient focusing in microchannels with embedded bipolar electrode. Lab Chip 9, 1903–1913, doi:10.1039/B822404H (2009).
Montgomery, R., Jia, X. & Tolley, L. Dynamic Isoelectric Focusing for Proteomics. Anal. Chem. 78, 6511–6518, doi:10.1021/ac060898w (2006).
Dai, J., Ito, T., Sun, L. & Crooks, R. M. Electrokinetic Trapping and Concentration Enrichment of DNA in a Microfluidic Channel. J. Am. Chem. Soc. 125, 13026–13027, doi:10.1021/ja0374776 (2003).
Wang, Y.-C., Stevens, A. L. & Han, J. Million-fold Preconcentration of Proteins and Peptides by Nanofluidic Filter. Anal. Chem. 77, 4293–4299, doi:10.1021/ac050321z (2005).
Lee, J. H., Song, Y.-A. & Han, J. Multiplexed proteomic sample preconcentration device using surface-patterned ion-selective membrane. Lab Chip 8, 596–601, doi:10.1039/B717900F (2008).
Liu, V., Song, Y.-A. & Han, J. Capillary-valve-based fabrication of ion-selective membrane junction for electrokinetic sample preconcentration in PDMS chip. Lab Chip 10, 1485–1490, doi:10.1039/B923214A (2010).
Liao, K.-T. & Chou, C.-F. Nanoscale Molecular Traps and Dams for Ultrafast Protein Enrichment in High-Conductivity Buffers. J. Am. Chem. Soc. 134, 8742–8745, doi:10.1021/ja3016523 (2012).
Wang, S., Hu, X. & Lee, L. J. Dynamic Assembly by Electrokinetic Microfluidics. J. Am. Chem. Soc. 129, 254–255, doi:10.1021/ja0666295 (2006).
Williams, S. J., Kumar, A., Green, N. G. & Wereley, S. T. A simple, optically induced electrokinetic method to concentrate and pattern nanoparticles. Nanoscale 1, 133–137, doi:10.1039/B9NR00033J (2009).
Chou, C.-F. et al. Electrodeless Dielectrophoresis of Single- and Double-Stranded DNA. Biophys. J. 83, 2170–2179, doi:10.1016/S0006-3495(02)73977-5 (2002).
Sasaki, N., Hosokawa, K. & Maeda, M. Alternating current cloud point extraction on a microchip for preconcentration of membrane-associated biomolecules. Lab Chip 9, 1168–1170, doi:10.1039/B901007F (2009).
Huber, D. E. & Santiago, J. G. Ballistic dispersion in temperature gradient focusing. Proc. R. Soc. A 464, 595–612, doi:10.1098/rspa.2007.0161 (2008).
Ross, D. & Locascio, L. E. Microfluidic Temperature Gradient Focusing. Anal. Chem. 74, 2556–2564, doi:10.1021/ac025528w (2002).
Lin, H., Shackman, J. G. & Ross, D. Finite sample effect in temperature gradient focusing. Lab Chip 8, 969–978, doi:10.1039/B713749D (2008).
Akbari, M., Bahrami, M. & Sinton, D. Optothermal sample preconcentration and manipulation with temperature gradient focusing. Microfluid. Nanofluid. 12, 221–228, doi:10.1007/s10404-011-0866-6 (2012).
Zhao, C. & Yang, C. Joule heating induced heat transfer for electroosmotic flow of power-law fluids in a microcapillary. Int. J. Heat Mass Transfer 55, 2044–2051, doi:10.1016/j.ijheatmasstransfer.2011.12.005 (2012).
Kim, S. M., Sommer, G. J., Burns, M. A. & Hasselbrink, E. F. Low-Power Concentration and Separation Using Temperature Gradient Focusing via Joule Heating. Anal. Chem. 78, 8028–8035, doi:10.1021/ac061194p (2006).
Sommer, G. J., Kim, S. M., Littrell, R. J. & Hasselbrink, E. F. Theoretical and numerical analysis of temperature gradient focusing via Joule heating. Lab Chip 7, 898–907, doi:10.1039/B701894K (2007).
Ge, Z., Yang, C. & Tang, G. Concentration enhancement of sample solutes in a sudden expansion microchannel with Joule heating. Int. J. Heat Mass Transfer 53, 2722–2731, doi:10.1016/j.ijheatmasstransfer.2010.02.033 (2010).
Ge, Z., Wang, W. & Yang, C. Towards high concentration enhancement of microfluidic temperature gradient focusing of sample solutes using combined AC and DC field induced Joule heating. Lab Chip 11, 1396–1402, doi:10.1039/C0LC00421A (2011).
Huang, Y. et al. Electric Manipulation of Bioparticles and Macromolecules on Microfabricated Electrodes. Anal. Chem. 73, 1549–1559, doi:10.1021/ac001109s (2001).
Cong, H., Yu, B., Tang, J., Li, Z. & Liu, X. Current status and future developments in preparation and application of colloidal crystals. Chem. Soc. Rev. 42, 7774–7800, doi:10.1039/c3cs60078e (2013).
Zhao, Y., Zhao, C., He, J., Zhou, Y. & Yang, C. Collective effects on thermophoresis of colloids: a microfluidic study within the framework of DLVO theory. Soft Matter 9, 7726–7734, doi:10.1039/C3SM27720H (2013).
Marcos, Y. C., Wong, T. N. & Ooi, K. T. Dynamic Aspects of Electroosmotic Flow in Rectangular Microchannels. International Journal of Engineering Science 42, 1459–1481, doi:10.1016/j.ijengsci.2003.07.012 (2004).
Kale, A., Patel, S., Hu, G. & Xuan, X. Numerical modeling of Joule heating effects in insulator-based dielectrophoresis microdevices. Electrophoresis 34, 674–683, doi:10.1002/elps.201200501 (2013).
Sridharan, S., Zhu, J., Hu, G. & Xuan, X. Joule heating effects on electroosmotic flow in insulator-based dielectrophoresis. Electrophoresis 32, 2274–2281, doi:10.1002/elps.201100011 (2011).
Shah, J. J., Gaitan, M. & Geist, J. Generalized Temperature Measurement Equations for Rhodamine B Dye Solution and Its Application to Microfluidics. Anal. Chem. 81, 8260–8263, doi:10.1021/ac901644w (2009).
Piazza, R. & Parola, A. Thermophoresis in colloidal suspensions. J. Phys. Condens. Matter 20, 153102, doi:10.1088/0953-8984/20/15/153102 (2008).
Alois, W. Thermal non-equilibrium transport in colloids. Rep. Prog. Phys. 73, 126601, doi:10.1088/0034-4885/73/12/126601 (2010).
Zhou, Y., Yang, C., Lam, Y. C. & Huang, X. Thermophoresis of charged colloidal particles in aqueous media – Effect of particle size. Int. J. Heat Mass Transfer 101, 1283–1291, doi:10.1016/j.ijheatmasstransfer.2016.05.109 (2016).
Braibanti, M., Vigolo, D. & Piazza, R. Does Thermophoretic Mobility Depend on Particle Size? Phys. Rev. Lett. 100, 108303, doi:10.1103/PhysRevLett.100.108303 (2008).
Zhu, J. & Xuan, X. Dielectrophoretic focusing of particles in a microchannel constriction using DC-biased AC flectric fields. Electrophoresis 30, 2668–2675, doi:10.1002/elps.200900017 (2009).
Lewpiriyawong, N., Yang, C. & Lam, Y. Electrokinetically driven concentration of particles and cells by dielectrophoresis with DC-offset AC electric field. Microfluid. Nanofluid. 12, 723–733, doi:10.1007/s10404-011-0919-x (2012).
Acknowledgements
This work was supported by the Ministry of Education of Singapore under Grant No. RG97/13. C.Z. and Z.G. are also supported by the “Top Young Talent Support Plan” from XJTU and a PhD scholarship from NTU, respectively.
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C.Z. and Z.G. designed the experiment, formulated the theoretical model and carried out the data analysis. Z.G. drafted the first version of manuscript, C.Z. improved this version substantially. Y.S. contributed to the experiment design and writing. C.Y. proposed and supervised this work. All authors have read, discussed and agreed on the results of manuscript.
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Zhao, C., Ge, Z., Song, Y. et al. Electrokinetically driven continuous-flow enrichment of colloidal particles by Joule heating induced temperature gradient focusing in a convergent-divergent microfluidic structure. Sci Rep 7, 10803 (2017). https://doi.org/10.1038/s41598-017-11473-w
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DOI: https://doi.org/10.1038/s41598-017-11473-w
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