Refractive index matching (RIM) using double-binary liquid-liquid mixtures

Within the last decade microscopic multiphase flows have gained broad interest. An exact understanding of the underlying hydrodynamic interrelations is the key for successful reactor layout and reaction control. To examine the local hydrodynamic behavior, non-invasive optical measurements techniques like particle tracking velocimetry (PTV) or (micro)particle image velocimetry ((\textmu)PIV) are the method of choice, since they provide precise velocity measurement with excellent spatial resolution. Such optical approaches require refractive index matching (RIM) of the involved flow phases to prevent optical distortion due to light refraction and reflection at the interfaces. Established RIM approaches often provide a single one degree of freedom which is sufficient to match the RI of the flow phases solely. With that, the material properties ($Oh$ number) are fixed and the relevant dimensionless numbers ($Ca$, $Re$) may only be altered hydrodynamically or geometrically. To avoid expansive geometric scaling of the microchannels, we propose an approach using two binary mixtures (double-binary mixtures) to introduce an additional degree of freedom. The approach allows examining liquid-liquid two-phase flows at a distinct velocity while being able to change the material combination ($Oh$-Number). Therefore $Ca$ and $Re$ can be chosen individually and the RIM provides undisturbed optical access. We present 4 different binary mixtures to be used, e.g. with Taylor droplets. The relevant material parameters are successfully correlated to measurement data, which delivers a system of equations that determines the mass fractions and the velocities to address $Re$ and $Ca$ individually. A proof-of-principle for the proposed double binary mixture RIM-approach is successfully established using \textmu PIV raw images.

duce an additional degree of freedom. The approach allows examining liquid-liquid two-phase flows at a distinct velocity while being able to change the material combination (Oh-Number). Therefore Ca and Re can be chosen individually and the RIM provides undisturbed optical access. We present 4 different binary mixtures to be used, e.g. with Taylor droplets. The relevant material parameters are successfully correlated to measurement data, which delivers a system of equations that determines the mass fractions and the velocities to address Re and Ca individually. A proof-of-principle for the proposed double binary mixture RIM-approach is successfully established using µPIV raw images.

Introduction and Concept
Microfludic processes using liquid-liquid multiphase flows has gained great interest in the last decades (Zhao and Middelberg, 2011;Chou et al, 2015;Ahmed et al, 2018;Shi et al, 2019). The applications range from chemical (Kobayashi et al, 2006;Song et al, 2006;Kralj et al, 2007;Lang et al, 2012;Tanimu et al, 2017) to biological (Clausell-Tormos et al, 2008;Mazutis et al, 2013;Chen et al, 2014;Wolf et al, 2015;Hosokawa et al, 2017) and pharmaceutical applications (Kang et al, 2014;Piao et al, 2015). The large specific surface area in combination with well defined and allegedly easy-to-control flow structures promise a great potential for process intensification. Thus, optimal reactor design and controllability of the flow is key to raise this potential.
Deep insight into the hydrodynamic interaction of the distinct flow phases enables to tune e.g. the mass transfer rates towards more sustainable operation modes close to the optimal working point (Magnaudet and Eames, 2000;Ern et al, 2012). To achieve this, numerical simulation and CFD-calculations enable relatively easily a parameterized study of e.g. liquid-liquid Taylor flows (Luis A. M. Rocha and João M. Miranda and Joao B. L. M. Campos, 2017). Dimensionless numbers (Re, Ca) and material property ratios (Oh) can be set freely and independently to identify e.g. critical operation modes.
The dimensionless quantities are based on the material parameters of the continuous phase since it provides the wall contact and drives the flow of the disperse phase. The capillary number compares the viscous forces with the interfacial tension forces Ca " u 0 η c σ and it is based on the superficial velocity u 0 , the dynamic viscosity η c of the continuous phase and the interfacial tension σ. The Reynolds number relates the inertia forces to the viscous forces Re " ρ c u 0 d η c , where ρ c denotes the density of the continuous phase and d the diameter of the microchannel. The Ohnesorge number Oh " b Ca Re removes the hydrodynamic influences and solely remains as a material parameter. Please note that for macroscopic liquidliquid flows, the set of dimensionless variables changes with the growing influence of inertia and gravitational forces to Re, W e and M o " Bo Oh 2 . Where the Weber number W e " Ca Re represents the inertia forces compared to the interfacial tension forces. M o introduces the buoyancy dependence of the flow's material system (Araújo et al, 2012) when combining the Bond number Bo " ∆ρ g d 2 σ with the Ohnesorge number. Since buoyancy forces are small (Bo ! 1) in microfluidic applications, we base our RIM system on the Oh number only.
Preferably non-invasive experimental methods need to be applied to investigate the hydrodynamic behavior of liquid-liquid multiphase flows supporting the numerical findings. Even in microchannels, a high spatial resolution of an entire flow field is accessible with e.g. optical measurement techniques (Park and Kihm, 2006;Kinoshita et al, 2007;Khodaparast et al, 2013). However, undistorted optical access is necessary to avoid measurement deviation due to light refraction and reflection.
Often the hardware related refraction effects of the setup can be compensated for adjusting the experimental design e.g. avoiding curved surfaces and using of corrective optics. The curved interfaces of microscopic liquid-liquid flows are commonly counteracted applying refractive index matching with one degree of freedom (Miessner et al, 2008;Ma et al, 2014;Liu et al, 2017). A broad overview of possible liquid-liquid, as well as solid-liquid refractive index matching possibilities, is given in the works of Budwig (1994) and Wright et al (2017). Recently, several approaches have been made using refractive index matched systems to mimic special application cases like specific rheology for blood (Najjari et al, 2016;Brindise et al, 2018), high-density differences or for a buoyant jet (Clément et al, 2018;Krohn et al, 2018).
In microscopic liquid-liquid flows RIM with one degree of freedom allows matching the RI of one phase solely to the other. The material system of the phases like density, viscosity and interfacial tension are fixed for the desired RI. The governing dimensionless numbers such as Re, Ca may only be parameterized hydrodynamically (superficial flow velocity) or geometrically (microchannel diameter). The monetary effort to parameterize the diameter of the microchannel is high, while the velocity alters both quantities simultaneously.
Alternatively, surfactants could be added to change the interfacial tension of the material system solely. Surfactant concentration well below the critical micelle concentration does not significantly change the viscosity of the host phase. Albeit this approach indeed addresses Ca only, the use of surfactants introduces severe effects such as altering the hydrodynamics of the flow as well as its mass transfer properties.
We suggest an approach using two immiscible binary mixtures to match refractive indices (Saksena et al, 2015;Cadillon et al, 2016), i.e. adding an additional degree of freedom to the system by introducing a binary mixture for each of the liquid phases. The now flexible material system provides an entire range of RI to match the immiscible binary liquid mixtures optically. Hence, the simultaneous velocity related change of Ca and Re may be compensated for by adequately adapting the material composition of the mixtures (Oh).
We carefully determine the mass fraction dependent material properties of the involved mixtures, establish dedicated correlation functions and provide an optimization algorithm to calculate the necessary information to use this RIM system. A proof of principle is given using µPIV raw-images of two fluorescence particle-seeded microscopic Taylor flows at two Re and constant Ca at different channel heights.
Recently, the viscosity ratio of both flow phases λ is reported to influence the local hydrodynamics of microscopic Taylor droplets (Rao and Wong, 2018). However, their measurements are limited to a narrow parameter range without refractive index matching (Kovalev et al, 2018;Liu et al, 2017). Therefore, we suggest four combinations of well quantified double-binary mixtures for the disperse as well as the continuous phase. This allows to additionally alter the viscosity ratio of the flow phases by changing the flow system.

Material and Methods
Within this section, the choice of the basic mixture compounds, the experimental procedures to retrieve the properties of the fluids and the numerical approach are described. All measurements are referenced to mass fractions ξ to compensate non-linearities (e.g., excess volume while mixing or when preparing solutions).

Basic Mixture Compounds
For the binary mixtures of this work, we focused to mainly use nontoxic, nonhazardous, newtonian substances. A wide range of addressable refractive indices is accomplished, when mixing substances if high and and low RI in each phase. The polar phase is chosen to be aqueous for practical reasons. The range of RI of the aqueous binary mixture is defined when using either DMSO or glycerol as newtonian liquid to elevate the RI. The nonpolar phase is based on hexane, as it represents a tradeoff between a lower RI and hazardous properties. The nonpolar binary mixture is complemented by either anisole or sunflower-oil, which establishes a high RI range. Rheometry measurements show, that in the observed range sunflower-oil also behaves newtonian.
Combining the suggested aqueous mixtures properties with the non-polar systems, the viscosity ratio λ between the phases of the flow can be changed by either inverting the flow phases or changing the combination of the materials. For that reason, we introduce and characterize different binary mixtures for the polar as well as for the non-polar phase. Please note, the viscosity ratio cannot be chosen freely. However, it is possible to choose a ratio below or above unity to investigate the hydrodynamic consequences.
For low viscous mixtures with viscosity ratio below one, we use water/DMSO and n-hexane/anisole, while for high viscosity ratio we propose to apply water/glycerol and n-hexane/sunflower oil.
With these mixtures, we reach a broad range of refractive indices, laying between the pure substance's RI of n-hexane (RI " 1.3753) and glycerol/DMSO (RI « 1.47). The material properties of the binary mixtures (density, viscosity, interfacial tension), as well as the refractive, are given in Sec. 3.

Determination of material properties
The refractive indices of the used fluids are measured using a Krüss Abbe refractometer AR2008, temperated at 20°C. The refractive indices were measured using a light wavelength of 589 nm (Sodium D1-line) with three independent measurements each. The refractometer uses a liquid film between two prisms to measure the angle of total reflection, from which the refractive index is calculated. For volatile or liquids with low viscosity or low surface tension, no stable film forms between the prisms, which leads to a high deviation. For this reason, the refractive indices of the n-hexane/anisole system for high mass fractions of anisole could not be acquired reliably. Therefore literature data is used.
The interfacial tension of the double binary mixtures is measured using a Lauda TVT drop tensiometer with a syringe of 2.5 ml and a stainless steel capillary at a temperature of 20°C. The interfacial tensions are acquired using the volume drop method: A droplet is formed at a capillary tip. Based on the balance of buoyancy and surface tension the droplet pinches off into the continuous phase. The dispersed droplet is detected with a light barrier and the interfacial tension calculated from the droplet volume.
The interfacial tension is a time-dependent property for nonpure or mixed systems. Thus, as part of the measurement of the dynamic interfacial tension, droplets with differently aged interfacial area are formed. The interfacial tension for infinite time σ inf can be derived depending only on bulk diffusion of surface-active substances. Therefore the interfacial tensions are correlated following Wilkinson (1972) and Sinzato et al (2017). Within our work, the droplet formation times and therefore the surface age lie between 2.5 s and 60 s.
The light barrier, that detects the detachment of the ascending droplets, cannot work properly when the refractive indices are matched. Thus, we deliberately detune the mass fraction of the nonpolar phase such, that a sufficient detection difference between the refractive indices of both phases (∆RI " 0.01) exists. The droplet detachment, as well as the interfacial tension, are determined at these detuned fluid compositions. The actual interfacial tension for the matched case is then retrieved by linear interpolation using the lever rule. The linear interpolation is considered valid since only the mass fraction of one of both phases is varied and the change in the mass fraction is kept small.
The measurements of the viscosities for the volatile compounds (n-hexane/anisole) are performed using a Malvern Kinexus Ultra Plus with solvent trap, cone-plate setup, 1 degree opening angle and a stationary shear rate table 10 s -1 .. 100 s -1 with 5 % stationarity tolerance. The remaining measurements are performed using a Bohlin Rheometer CS and a 30 ml double-gap system. All measurements were performed at 20°C.
The densities of the mixtures are mostly retrieved from literature data.

Calculating mass-fractions and the superficial velocity
The main merit of the double-binary mixture flow system is the ability to address different Re and Ca independently of each other. Keeping in mind the definition of Re and Ca, this can be stated as an optimization problem with the superficial velocity u 0 as the target value. The mass fractions of the continuous phase ξ c and disperse phase ξ d are the control variable, which influences the material properties. If the fluid properties for the pure substances as well as for the mixtures are known, Ca and Re can be calculated. Because the user needs to establish the flow at a distinct Re and Ca, the equations can be changed such, that the superficial velocity u 0 for both numbers is a function of the continuous phase mass fraction ξ c : The problem defines as a minimization problem to find u 0 , where the difference of u 0,Ca´u0,Re « 0. Depending on the material property function (given in Sec. 3.1), the problem is not necessarily strictly monotonous. Therefore the use of numerical solvers is strictly advised. A working example using fminsearch from MATLAB is given in the supplementary resources. After input of the desired Re and Ca, this program automatically determines the necessary superficial velocity u 0 and mass fraction of both phases. For a minimum residuum of this optimization (u 0,Re " u 0,Ca ), the correct u 0 is known as well as the corresponding mass fraction of the continuous phase ξ c . The mass fraction of the disperse phase ξ d can be calculated via the refractive index of the continuous phase.

Experimental Results
Within this section, the material properties of the binary and RI-matched doublebinary mixtures are experimentally investigated.

Properties of binary mixtures
To solve the optimization problem, a solver needs a steady optimization function to work with. However, the measurement data consists of discrete points including a measurement error: A transition of the discrete data sampling to continuous functions is necessary. Thus, we correlate the data with polynomial approaches for simplicity.
The equation for a polynomial function follows where y is the desired property (e.g., density, viscosity or interfacial tension), ξ the mass fraction of the mixture and A 3 -A 0 fitting coefficients for the polynomial. The polynomial coefficients for the different material properties as well as the experimental data and the range of validity are shown in the following.
At first, the densities of the binary mixtures are investigated in Fig. 1 a) for the polar and in Fig. 1 b) for the nonpolar media. The system water/glycerol shows a nearly linear behavior, while the system water/DMSO shows a peak at approximately ξ " 0.8. This is caused by nonlinear mixing behavior due to the similarity of water/DMSO and also affects the viscosity. The system n-hexane/anisole shows a nearly linear behavior, while n-hexane/sunflower oil shows a deviation from linearity. The correlations extracted from the measurement and literature data are shown in Tab. 1.
In Fig. 2 the refractive index of the water/glycerol mixture features a linear behavior (empty squares), while water/DMSO shows a nonlinearity for higher  DMSO mass fractions (Fig. 2 a) , triangles). For the nonpolar substances the system n-hexane/sunflower-oil (filled squares) behaves nearly linear, while n-hexane/anisole (filled triangles) increases the slope indicating non-linear dependence (Fig. 2 b) ). For all mixtures, the measurements confirm the available literature data. The correlation coefficients are shown in Tab. 2. The viscosities of the four binary mixtures are given in Fig. 3. Both of the highly viscous mixtures (water/glycerol Fig. 3 a) and hexane/sunflower-oil Fig. 3  d) ) exhibit similar behavior. As intended, with a higher mass fraction of the more viscous substances, the viscosity rises. The less viscous mixtures water/DMSO (Fig. 3 b) ) and n-hexane/anisole (Fig. 3 c) ) show different behavior. While the viscosity of n-hexane/anisole mixtures increases quadratically with a rising   (2005), upside triangles, own measurements) and n-hexane/sunflower oil (filled squares, own measurements) mass fraction of anisole, the viscosity of water/DMSO reaches a peak at ξ " 0.70. For n-hexane/anisole no own measurements could be performed, since the high evaporation rate of the volatile hexane/anisole mixture leads to a significant deviation in the mass fraction of the mixture during the measurement. Instead, literature data is used. The correlation coefficients are shown in Tab. 3.

Properties of RI-matched double-binary mixtures
In addition to the direct properties of the individual binary mixtures that have been discussed in the previous section, the properties of the coupled RI-matched material systems (double-binary mixtures) are discussed in this section. Since the double-binary system consists of four substances, the interfacial tension is influenced independently and possibly nonlinearly by the mass fractions of both binary mixtures. Thus to obtain a manageable experimental effort for the required measurements, the interrelations are linearized and the system is simplified: For the use in RI-matched measurements, only the mass fractions of the matched solution need to be observed. As it is visible in Fig. 4 and 5 this simplifies the problem to two-dimensional problem.
To retrieve the specific mass fractions of both phases for the matched case, the correlations for the RI of both phases are equated and a fit function is numerically retrieved. The behavior of the RI-matched double-binary systems is a combination of the binary mixtures. The results are shown for all double-binary mixture systems in Fig. 4.
The system water/DMSO-hexane/anisole (Fig. 4 (c)) shows the most prominent nonlinear behavior. This is caused by the larger increase of the RI of anisole for elevated anisole mass fractions and the nonlinearity of water/DMSO. For the system water/glycerol-n-hexane/anisole ( Fig. 4 (a)) this behavior is as not prominent since the binary mixture water/glycerol in contrast to water/DMSO is nearly linear. As expected from the binary mixture's behavior, this also holds for the system water/glycerol-hexane/sunflower-oil ( Fig. 4 (b)), while again caused by water/DMSO, for water/DMSO-n-hexane/sunflower-oil nonlinearities are present at higher DMSO mass fractions ( Fig. 4 (d)). The correlation coefficients for the matched systems are shown in Tab. 4. Additionally to the refractive index, the densities, interfacial tension and viscosities for the different matched mass fraction have to be considered for the calculation of the desired dimensionless quantities (Re, Ca, λ). Every matched system consists of two binary mixtures with exactly one RI for the matched case and one specific mass fraction and viscosity for the polar as well as the disperse phase. Changing the mass fraction of one phase, the mass fraction of the other phase needs to be adjusted to keep the RI matching. This changes the viscosity ratio, as it also depends on the ratio of the binary mixtures of each phase.
For the determination of the dimensionless quantities Re, Ca, Oh of microscopic two-phase flows, especially the viscosity of the continuous phase is important, since it influences the dimensionless quantities the strongest. Therefore the viscosities for the continuous phase of the high viscous systems are shown (Fig.  5).
At first, the polar phase is depicted as the continuous phase, resulting in the graphs of Fig. 5. The combinations with water/glycerol show a broad range of available continuous phase viscosities. Considering the viscosities of both flow phases, the viscosity ratio λ of the respective RI-matched material systems can be calculated. The results are shown in Fig. 6 separated for polar and nonpolar continuous phase: In Addition to the determination of the material properties that depend only on the binary mixtures themselves, also the interfacial tension needs to be described. Since it depends on the forces of the energetic state of the interfacial area, the determination for a quarternary fluid system is complex. For the following measurements, only the interfacial tension of the RI-matched case is of interest. Thus, we only determine values at the mass fractions of the RI-matched interfacial tensions to minimize the experimental effort. Due to the measurement restrictions (see in Sec. 2.2), we perform the measurements at slightly detuned refractive indices and linearly interpolate the interfacial tension for the matched case between the results. The measurement data, as well as the derived correlations, are shown in Fig. 7.
The interfacial tension between the RI-matched liquids exhibits different behavior for each system. The system water/glycerol-hexane/anisole (Fig. 7 a)) shows an unpredictable interfacial tension development for rising mass fractions of glycerol or anisole. The interpolated values of the single measurements deviate around the correlation function. This is a sign for strong nonlinear interrelations between the four substances. Probably caused by weaker intermolecular forces between glycerol and anisole depending on the composition of the mixture. The system water/glycerol -hexane/sunflower-oil shows a minimum for equivalent fractions of all four substances (ξ p « 0.5, ξ n « 0.5), while the interfacial tension increases for higher amounts of glycerol or sunflower oil (Fig. 7 b)).
The systems involving water/DMSO expose a decreasing interfacial tension with decreasing mass-fraction of n-hexane. Especially the water/DMSO -hexane/anisole shows a very low interfacial tension for lower mass fractions of hexane (Fig. 7 c)), which is caused by a diminished structural difference to hexane. Water/DMSO -n-hexane/sunflower-oil shows a similar decrease of the interfacial tension (Fig. 7 d)).
The most significant deviations (Fig. 7 a) and b)) are situated in a range of 2 mPas. Please note, that the derived fitting function represents an averaging attempt to describe the complex 4-material-system. Therefore, a deviation between the correlation and the interpolated data of single measurements can be caused by either the linearization or confined effects at distinct mass fractions as well as measurement errors. Since the results of the single measurements are based on at least 20 independent droplets (5 droplets x 4 formation times), we consider possible measurement errors to attribute from diminutive contaminations of the water/glycerol -n-hexane/sunflower-oil c) water/DMSO -n-hexane/anisole d) water/DMSOn-hexane/sunflower-oil. Actual measurements (squares) are used to interpolate (bars) the interfacial tension at the matched phase composition (circles). The correlation for the matched interfacial tension is the correlated (bold line). Each measurement consists of 5 droplet formation cycles at different droplet formation times. Within each cycle, at least 5 droplets are formed to ensure reproducibility volume tensiometer. The correlation coefficients for the interfacial tension for all four systems are shown in Tab. 5.

Discussion
Based on the material properties of the binary mixtures as well as the doublebinary mixtures, which were experimentally determined and successfully modeled with polynomial correlations, we describe the features of the double-binary approach in this section and deliver a proof-of-principle.

Features and limits of the double-binary approach
The proposed double-binary mixture approach allows tuning the material system of e.g. microscopic Taylor flows with an additional degree of freedom. A two-phase flow can now be RI-matched at a specific individually set of Re and Ca individually. This is done via a variation of the mass-fraction of both phases ξ c , ξ d and the superficial velocity u 0 . Alternatively, a set of fixed Ca/Re ratios (" Oh) at distinct RI can be adjusted, allowing to match the system to a specific reactor material. In this way even complex structures or three phase flows can be observed once the flow is matched to the reactor material. Additionally, the flow can be applied at a specific viscosity of the continuous phase (if fluids with a distinct viscosity should be modeled). A graphical representation of the capabilities is given in Fig. 8.
Double-binary mixture specific Re and Ca specific Oh specific η specific RI for three-phase matching λ can be changed by altering the flow system c Fig. 8 Features of the double-binary fluid system. Depending on the case of application, Re and Ca can be adjusted individually. Alternatively, a defined continuous phase viscosity ηc, a defined RI or a defined Oh can be chosen. The latter three can only be addressed at a defined Re or Ca, while the other dimensionless quantity is fixed Based on the conducted measurements and literature data, the proposed doublebinary mixture systems are sufficiently described to calculate the relevant dimensionless quantities Ca and Re for all accessible mass fractions and superficial velocities. These latter two quantities can be calculated by the MATLAB program we supply with the supplementary material. Alternatively, they mass fraction and the superficial velocity can be retrieved graphically from the nomograms presented in Fig. 9. The desired Ca and Re are chosen on the according axis and the corresponding matched Oh and RI of both phases, as well as the superficial velocity, can be received. The RI determines the mass fractions of both phases ξ (Fig. 4) and the associated viscosity ratio (Fig. 6). Via the continuous phase viscosity (Fig. 5) and λ the disperse phase viscosity can be determined. Generally, the systems with a high viscous continuous phase (Fig. 9 a) + b)) cover a larger range of possible Ca and Re, while for the lower viscous continuous phase the parameter range is smaller.  (d) Fig. 9 Nomograms for reachable Ca and Re numbers for a polar continuous phase. a) water/glycerol -n-hexane/anisole b) water/glycerol -n-hexane/sunflower-oil c) water/DMSOn-hexane/anisole d) water/DMSO -n-hexane/sunflower-oil

Proof of Principle
The practicability of the proposed approach for optical measurements and especially the possibility to reach the desired Re and Ca independently while a matched refractive index is proven in an experimental approach. A microscopic Taylor flow is established at two different Re numbers while Ca is held constant. The experimental setup to record the PIV raw-images is described in the appendix.
The capability of the double-binary approach and the quality of refractive index matching is evaluated in three measurement planes at two Re numbers at a steady Ca. Measurements in the symmetry plane (channel center plane), the channel top wall and at an intermediate plane at 0.75 of the channel height are carried out (Fig. 4.2). In the symmetry plane at the half channel height, distortions arising from non-ideal refractive index matching accumulate and can be quantified. The measurements at the channel top allow classifying, if the flow through the gutters can be measured. Within the µPIV raw images, the droplet interface is not visible. The rawimages in Fig. 11 show clearly that the droplet length decreases when the focal plane is moved towards the channel top. This is caused by the curvature of the droplet interface. Only the tracer particles in the focal plane are displayed sharp, while particles on other planes out of focus introduce a blurry signal. Thus, the correlations for the refractive index as well as the solver algorithm works well.
Taylor flows were established and recorded without optical distortion. Thus, the proposed double-binary mixture method works well.

Conclusion
Within this study, we present and successfully validate a new approach using double-binary mixtures for both immiscible flow phases to establish a refractive index matched microscopic multiphase flows. In comparison to classical monobinary mixture approaches, Re and Ca can be addressed individually in a material restricted parameter set, since viscosity and interfacial tension (and thus the different flow forces) do not change in the same order of magnitude if the mass fractions of the phases' binary mixtures are varied. Alternatively, multiphase flows at different Oh at a fixed RI can be established to match the reactor material (e.g. simulating three-phase flows via monolith). Additionally, we introduce two binary mixtures for a polar and nonpolar phase to enable the investigation of e.g., different viscosity ratios λ or flow systems with simultaneously high or low viscosities are possible too.
Measurements for the relevant material properties (densities, viscosities, refractive index) of the binary mixtures as well as the RI-matched compositions (interfacial tensions) are carried out and compared to literature data to characterize the system. The task to establish multiphase flows at specific Re and Ca independently is identified as an optimization problem and the material properties as well as the interfacial tension are successfully described with correlations that allow the use of a solver algorithm.
In first measurements, the capability to establish refractive index matched Taylor flows at freely chosen Ca and Re is proven. This proof of principle is successfully conducted using recorded µPIV raw images. With the proposed double-binary RIM-approach the specific influences on the local velocity of droplets can now be independently examined via optical flow visualization techniques (PTV, PIV).
1.034µm) to receive a high resolution in the z-direction. A pulsed Nd:YAG laser (New Wave Research Solo-PIV III ) with a 15 Hz repetition rate, 50 mJ pulse intensity and a pulse length of 3 ns -5 ns with frequency doubling (wavelength: λ ex = 532 nm) serves as a light source for the measurement. Images of the flow are acquired using an active-cooled high quantum-efficient PCO.sensicam qe 670 LD 3078 double CCD-camera with an acquisition rate of 4 Hz at a resolution of 1376 px x 1040 px. The continuous phase is seeded with particles of 1.61 µm particles. The particles are coated with FluoRed as fluorescence dye (excitation peak 530 µm, emission peak 607 µm) and are dispersed in the water/glycerol phase using an ultrasonic bath for 15 min at 20°C.
Two syringe pumps (Dolomite Mitos Duo XS ) supply a steady flow such, that the volume flow of both phases can be individually controlled. The excitation light from the pulsed Nd:YAG laser is guided into the Zeiss LSM210 microscope and the laser is widened with a convex lens of short focal length. The illumination is additionally averaged with a holographic diffuser.
A dichroic mirror separates the green excitation light from the red fluorescence light and directs it to the camera. To further improve the cutoff, an additional longpass filter is mounted in the light-path to shield the camera from laser light (Fig.  12). A timing unit synchronizes the laser and the camera. An overview of the experimental and optical parameters is given in Tab. 6.