Skip to main content
Micromachines logoLink to Micromachines
. 2026 Feb 11;17(2):234. doi: 10.3390/mi17020234

CFD Simulation and Structural Optimization Analysis of Micromixing Processes in T-Shaped Microreactors

Yongzhi Ning 1, Bo Wang 1, Runci Wang 1, Taihong Yan 1,*
Editor: Kwang-Yong Kim1
PMCID: PMC12943166  PMID: 41753894

Abstract

Microreactors offer remarkable advantages in intensifying mixing/mass transfer and hold promising prospects for industrial applications. In this study, T-shaped microreactors (TMRs) integrated with baffle, orifice-plate, and venturi structures (featuring different contraction angles) were designed. Based on the Villermaux–Dushman reaction system, three-dimensional computational fluid dynamics (CFD) models were established to simulate the fluid flow and mixing-reaction processes in these microreactors. The results demonstrate that peaks in velocity, turbulent kinetic energy, and turbulent dissipation rate consistently emerge in the confluence region of the two fluid streams. In the operating range of this study, the baffle configuration exhibits the highest micromixing performance but also induces the largest pressure drop, followed by the orifice-plate structure. Notably, the venturi structure not only enhances micromixing efficiency but also results in a minimal increase in pressure drop and eliminates flow dead zones. Specifically, the venturi structure with a 45° contraction angle achieves a balance between energy consumption and micromixing efficiency. Using the agglomeration model, the micromixing times of the microreactors with various structures were determined to range from 0.025 to 0.234 ms.

Keywords: microreactor, micromixing, computational fluid dynamics (CFD), process intensification, venturi structure

1. Introduction

Microreactors possess distinct advantages, including a large specific surface area, small volume, low mass transfer resistance, and facile controllability, which facilitate rapid fluid mixing/mass transfer, improved reaction efficiency, and enhanced product quality [1,2]. As a result, they have been extensively applied in various fields such as nanoparticle synthesis [3,4], organic synthesis [5,6], biomedicine [7,8], and energy generation [9,10].

Microreactors are primarily categorized into two types: active and passive. Active microreactors rely mainly on external energy inputs, such as electric fields [11], magnetic fields [12], and acoustic fields [13], to drive fluid mixing [14,15]. Tang et al. [16] and Qian et al. [17] employed electric and magnetic fields for micromixer actuation, respectively, enhancing mixing intensity by inducing eddy currents to promote convective diffusion. With the deepening of research, active microreactors are evolving toward precise regulation. Yang et al. [18] proposed a mixing strategy based on suspended magnetic microrobots, and numerical simulations verified that this approach can significantly improve mixing performance. However, active systems generally require complex external driving devices, which restricts their large-scale application. Although Kazemi et al. [19] achieved precise control of mixing quality by optimizing parameters of a periodically potential-driven electroosmotic micromixer via numerical simulations, this limitation has not been fundamentally addressed.

In contrast, passive microreactors enhance mixing through internal structural design, utilizing mechanisms such as fluid chaotic convection [20] and shear effects [21,22]. Due to their advantages of simple structure, high stability, easy integration, and low energy consumption, passive microreactors have become a research focus. Furthermore, the advancement of additive manufacturing technology provides an efficient solution for fabricating their complex structures [23]. Studies on traditional structures (e.g., Tesla structures, wall-grooved structures) are relatively mature. Both Lai et al. [24] and Yang et al. [25] adopted Tesla structures to intensify mixing in microreactors. Wu et al. [26] incorporated grooves and protrusions on the microreactor wall to disrupt the stable boundary layer flow, thereby enhancing mixing efficiency.

In recent years, novel passive structures (e.g., fractal channels, periodic disturbance units, and split-recombine structures) have emerged. Related research heavily relies on CFD simulations for mechanism analysis and structural optimization. Amrendra et al. [27] compared the mixing performance of microchannels with staggered and opposed obstacle units. Movahed et al. [28] established a prediction model for liposome properties in a periodically disturbed mixer based on response surface methodology. Shao et al. [29] investigated the mixing process of a split–recombine microreactor via numerical simulations, providing a basis for structural optimization.

Focusing on TMRs, experimental and numerical simulation studies on their micromixing performance have progressively advanced. Researchers commonly employ the Villermaux–Dushman competitive reaction system to characterize micromixing efficiency, investigating the effects of parameters (e.g., flow rate, fluid viscosity, and inlet structure) on mixing performance [30]. Abiev et al. [31] confirmed that a two-stage strong swirling microreactor exhibits superior mixing efficiency and pressure drop characteristics compared to a TMR, indicating substantial room for improving the mixing performance of TMRs. With the rapid development of computing power and simulation models, CFD has been widely used to simulate flow, mixing/mass transfer, and reaction processes, revealing underlying mechanisms and structural design principles [32,33]. Soleymani et al. [34] demonstrated through CFD simulations that structural dimensions and operating parameters significantly influence the flow and mixing performance of TMRs. Aoki et al. [35] numerically studied the effects of internal structures (e.g., channel confluence and bending) on mixing performance. Ouyang et al. [36] established a CFD model for mixing-reaction processes in a double-tube microreactor, employing the probability density function (PDF) model and finite-rate/eddy dissipation model to describe the micromixing process, respectively. This model enabled the acquisition of reactant/product distribution characteristics and micromixing efficiency. Dong et al. [37] controllably synthesized mesoporous FePO4nanoparticles using an ultrasound-enhanced turbulent T-junction microreactor (UTISR). Combined with experimental validation and CFD simulations, they systematically explored the synergistic effect of impinging flow and ultrasonic radiation on mesoporous structure formation. Mariotti et al. [38] confirmed that flow unsteadiness in TMRs significantly affects reaction yield. Unsteady asymmetric flow patterns can increase yield by over 30%, whereas unsteady symmetric flow patterns exert the opposite effect, offering valuable insights for process intensification.

Despite the extensive use of CFD simulations in microreactor design, most existing models inadequately address the trade-off between micromixing efficiency and energy consumption. In this study, based on the Villermaux–Dushman reaction system, three-dimensional CFD models were established to characterize the fluid flow and mixing-reaction processes in TMRs with different internal structures. The developed three-dimensional CFD models were validated using experimental data, and the model parameters were determined accordingly. Under different Reynolds number conditions, the effects of internal structures (including baffles, orifice plates, and venturi tubes with various contraction angles) on the velocity distribution, turbulent kinetic energy, turbulent kinetic energy dissipation rate, and component concentration distribution inside the microreactors were systematically investigated. Meanwhile, the pressure drop and segregation index of various microreactors were obtained. Subsequently, the characteristic micromixing time was calculated by adopting the agglomeration model.

2. Materials and Methods

2.1. Geometric Model

The TMR features a rectangular channel cross-section. The two inlet channels are 20 mm in length and 0.6 mm in width, while the mixing channel is 40 mm in length and 1.2 mm in width. All channels have a uniform depth of 0.6 mm (Figure 1). To enhance the mixing of the two fluid streams, baffle-type obstacles, orifice-plate structures, and venturi structures (with contraction angles of 30°, 45°, 60°, and 75°) were integrated into the mixing region. The contraction port size of all venturi structures was uniformly set to 0.6 mm. The enhanced structures and their dimensions are illustrated in Figure 2. Hereafter, the microreactors with different structures are denoted as follows: B-TMR (baffle-type), O-TMR (orifice-plate-type), V30-TMR (venturi with 30° contraction angle), V45-TMR (venturi with 45° contraction angle), V60-TMR (venturi with 60° contraction angle), and V75-TMR (venturi with 75° contraction angle).

Figure 1.

Figure 1

Schematic diagram of the TMR.

Figure 2.

Figure 2

Enhanced structures of the TMR: (a) B-TMR; (b) O-TMR; (c) V30-TMR; (d) V45-TMR; (e) V60-TMR; (f) V75-TMR.

2.2. Model Equations

2.2.1. Governing Equations

The CFD simulation involves liquid flow and chemical reactions, requiring the solution of the continuity equation, momentum equation, and species transport equation. The reactor operates under steady-state, single-phase continuous flow conditions, and the fluid is assumed to be incompressible. The relevant governing equations are as follows:

Continuity equation:

ρU=0 (1)

Momentum conservation equation:

ρUUμU+UT23UI=p (2)

Species transport equation:

ρUφα=Jα+Sα (3)

For turbulent flow, the diffusion flux Jα is expressed as:

Jα=ρDα,m+μtSctφα (4)

where φα is the local mass fraction of species α; Jα is the diffusion flux of species α; Dα,m is the mass diffusion coefficient of species α in the mixture; Sct is the turbulent Schmidt number; and μt is the turbulent viscosity.

The standard k-ε two-equation turbulence model with an extensible wall function was used for model closure:

Turbulent kinetic energy (k) equation:

tρk+xiρkui=xjμ+μtσkkxj+Gk+GbρεYM+Sk (5)

Turbulent dissipation rate (ε) equation:

tρε+xiρεui=xjμ+μtσεεxj+C1εεkGk+C3εGbC2ερε2k+Sε (6)

where ρ is the fluid density; ui is the velocity component in the xi direction; Gk and Gb are the turbulent kinetic energy generation terms due to the mean velocity gradient and buoyancy, respectively; YM is the turbulent kinetic energy dissipation term caused by fluctuating expansion in compressible turbulence; Sk and Sε are the source terms for k and ε, respectively. The model constants were set as follows: C1ε=1.44, C2ε=1.92, σk=1.0, σε=1.3.

2.2.2. Finite-Rate/Eddy Dissipation Model

For fast reaction systems, the actual reaction rate is controlled by component mixing rather than intrinsic kinetics. In the Eddy Dissipation Model (EDM), the reaction rate is determined by the smaller value between the mixing-controlled rate (calculated via EDM) and the kinetics-controlled rate (calculated via intrinsic kinetics). The species with the lowest concentration dominates the actual reaction rate.

EDM-based reaction rate:

Ri,r=vi,rMiAmρεkminY1v1,rM1,Y2v2,rM2,,Ynvn,rMn (7)

Kinetics-based reaction rate:

Ri,r=kf,rj=1N Cj,rmkb,rj=1N Cj,rn (8)

where νi,r is the stoichiometric coefficient of species i in reaction r; Mi is the molar mass of species i; Yi is the mass fraction of species i; Am is an empirical constant obtained by fitting simulation results; kf,r and kb,r are the forward and backward reaction rate constants for reaction r, respectively; and Cj,r is the concentration of species j in reaction r.

2.3. Micromixing Reaction System

The Villermaux–Dushman parallel competitive reaction system [39] has been widely used for micromixing research [40,41] because of its flexibility and convenience. Based on this method, the segregation index can be defined to characterize the micromixing efficiency, analyze the micromixing processes, and optimize the operational parameters in reactors [42,43]. The iodate–iodide parallel competitive reaction system is widely used to evaluate liquid micromixing efficiency in reactors. This system includes a fast neutralization reaction, a redox reaction, and an iodine complexation reaction, with the following reaction equations:

R1 (Neutralization reaction):

H2BO3+H+k1H3BO3 (9)

R2 (Redox reaction between iodide and iodate ions):

5I+IO3+6H+k23I2+3H2O (10)

R3 (Iodine complexation reaction):

I+I2k4k3I3 (11)

The reaction constants for R1 and R3 are k1=1011 m3/(kmols), k3=5.9×109 m3/(kmols), and k4=7.5×109 s1.

At room temperature, the intrinsic kinetics of the competitive reaction (R2) between iodide and iodate ions remains controversial [44,45], but most studies classify it as a 5th-order reaction. The reaction rate is expressed as:

r2=k2IO3I2H+2 (12)

where k2 is the reaction rate constant, with different expressions depending on the ionic strength (I) [46]:

For I<0.166M,log10k2=8.3831.5112I+0.23689.

For I0.166M,log10k2=9.281053.664I.

The segregation index XS, calculated from the by-product concentration, quantifies micromixing performance:

XS=0: Ideal mixing (only the main reaction occurs).

XS=1: Complete segregation (only the side reaction occurs).

The calculation formulas for XS are:

XS=YYST (13)
YST=6IO306IO30+H2BO30 (14)
Y=2Vbuffer +Vacid I2+I3Vacid H+0 (15)

In the experiment, the main reactant H2BO3 is in excess. If mixing is complete, H+ is fully consumed by the main reaction, and no I2 or I3 is generated (XS = 0). Otherwise, both R2 and R3 will occur, and the XS ranges between 0 and 1.

2.4. Mesh Model and Mesh Independence Verification

Structured meshes were generated for all microreactors using ICEM. Figure 3 shows the mesh independence verification of the TMR at Re=2000. When the mesh count exceeds 180,000, the segregation index and pressure drop from the simulation remain nearly constant. Thus, a mesh model with 389,100 elements was adopted for subsequent calculations. The mesh count and quality for microreactors with different structures are listed in Table 1. Schematic diagrams of the mesh models for microreactors with different structures are shown in Figure 4.

Figure 3.

Figure 3

Mesh independence verification of the TMR at Re = 1800.

Table 1.

Mesh count and quality of each microchannel reactor.

Microreactor Type Mesh Count Minimum Mesh Quality
TMR 389,143 1
B-TMR 508,369 0.98
O-TMR 524,830 0.97
V30-TMR 453,816 0.87
V45-TMR 502,820 0.71
V60-TMR 410,254 0.81
V75-TMR 451,000 0.95

Figure 4.

Figure 4

Schematic diagrams of the model mesh; (a) TMR; (b) B-TMR; (c) O-TMR; (d) V60-TMR.

2.5. Boundary Conditions and Solution Method

Due to the stability of liquid flow in microchannels, the steady-state simulation method is used in this paper. Fluid A and Fluid B enter from the two inlet channels, respectively, with velocity inlets specified at the inlets. The hydraulic diameter was calculated using D = 4A/l, where A is the cross-sectional area and l is the wetted perimeter, and the turbulence intensity was calculated using I = 0.16Re−1/8. The outlet was set as a pressure outlet with atmospheric pressure.

The convergence criteria were set as follows: 103 for the continuity and momentum equations, and 105 for the species transport equation. During the simulation, the concentrations of I2, I3, H3BO3, and H+ were monitored. All simulations were performed using ANSYS Fluent 19.0 (ANSYS Inc., Canonsburg, PA, USA), with the discretization methods for key variables listed in Table 2.

Table 2.

Discretization methods for key variables.

Variable Discretization Method
Momentum Equation QUICK
Turbulent Kinetic Energy Third-Order MUSCL
Turbulent Dissipation Rate Third-Order MUSCL
Pressure–Velocity Coupling Coupled
Pressure PRESTO

The operating parameters and constants used in this study were listed in Table 3.

Table 3.

Operating parameters and constants in this study.

Parameter/Constant Symbol Value Unit
Inlet flow rate V in 16.25–92 mL/min
Reynolds number of the mixing channel Re 600–3400
Volume flow ratio R 1:1
Initial concentration of H+ c H+,0 0.1 mol/L
Initial concentration of H2BO3 c H2BO3−,0 0.3636 mol/L
Initial concentration of I c I−,0 0.01167 mol/L
Initial concentration of IO3 c IO3−,0 0.00233 mol/L
Molecular diffusion coefficient D 2 × 10−9 m2/s
Density ρ 997 kg/m3
Dynamic viscosity μ 0.89 mPa·s

3. Results

3.1. Experimental Verification of the Microreactor

To validate the turbulence model and determine the parameters of the EDM, we conducted pressure drop and micromixing experiments in a TMR. The experimental methodology was consistent with that reported in Reference [47], and the reactant concentrations were identical to those employed in the simulations.

The pressure drop measured under different flow conditions was used to verify the turbulence model. Figure 5a shows the comparison of pressure drop simulation values with experimental data using different turbulence models. The standard k-ε model shows the largest error, while the standard k-ε model with an extensible wall function and the Transition SST model exhibit smaller errors. At medium-to-high Reynolds numbers (Re > 2000), the standard k-ε model with an extensible wall function shows better agreement with experimental data (a relative error ≤ 25%) and was thus adopted for subsequent simulations. Figure 5b shows that the error between the simulated and experimental XS values is within 15%. In this paper, the fitting relationship between Am and Re (shown in Figure 6) was used to determine Am under different flow rates, with the fitting function expressed as Equation (9) and a goodness of fit R2=0.998.

A=4571Re1.597+0.8313 (16)

Figure 5.

Figure 5

(a) Comparison of simulated pressure drop values (different turbulence models) with experimental data; (b) comparison of simulated and experimental XS values under different flow rates.

Figure 6.

Figure 6

Fitting curve between Re and Am.

3.2. Flow Field Characteristics in Microreactors with Different Enhanced Structures

Figure 7 shows the velocity distribution characteristics of TMRs, B-TMRs, O-TMRs, and V60-TMRs at Re=1600. In the unstructured microreactor (TMR), the two fluid streams converge and contract into the mixing channel, with a maximum velocity of 3.35 m/s. In the B-TMR, the flow velocity in the mixing channel fluctuates continuously after confluence, reaching a maximum of 8.86 m/s. In the O-TMR, the fluid undergoes sudden contraction followed by re-separation, with a maximum velocity of 6.22 m/s. In the V60-TMR, the fluid contracts and expands gradually, with a maximum velocity of 4.26 m/s (slightly higher than that of the TMR). Compared with the other three structures, the venturi’s contraction–expansion design guides fluid flow without obvious boundary layer separation, i.e., without the occurrence of obvious dead zones.

Figure 7.

Figure 7

Velocity contour maps under different enhanced structures: (a) TMR; (b) B-TMR; (c) O-TMR; (d) V60-TMR.

Figure 8 shows the distribution characteristics of turbulent kinetic energy and turbulent dissipation rate along the tube length. Similarly to the velocity peaks, the baffle structure exhibits the highest peaks of turbulent kinetic energy and dissipation rate, followed by the orifice-plate structure. The V60-TMR and TMR show significantly lower values. In the first 3 mm of the mixing channel, the baffle structure exhibits two peaks (one large, one small) in turbulent kinetic energy and dissipation rate. This is because the baffle causes two major changes in flow direction and cross-sectional area, as shown by the two maximum velocity regions in the velocity contours. This indicates that the baffle and orifice-plate structures induce higher turbulence intensity due to continuous flow path perturbations in the confluence region, resulting in higher energy consumption.

Figure 8.

Figure 8

Distributions of (a) turbulent kinetic energy and (b) turbulent dissipation rate along the tube length (different enhanced structures) at Re = 1600.

Figure 9 shows the effect of Re on pressure drop in four types of TMR. For all structures, pressure drop increases with Re: the baffle structure shows the steepest increase, while TMR and V60-TMR show gentle increases. At the same Re, the pressure drop follows the order: B-TMR > O-TMR > TMR ≈ V60-TMR.

Figure 9.

Figure 9

Effect of Re on pressure drop (different enhanced structures).

3.3. Micromixing Efficiency of Microreactors with Different Enhanced Structures

Figure 10 shows the distribution characteristics of H+ and H2BO3 concentrations in the four microreactors. The baffle structure induces the fastest key reactant (H+) consumption (nearly complete at 1.2 mm from the mixing point) due to high turbulence intensity. The orifice-plate structure follows, while TMR and V60-TMR show similar H+ distribution patterns (V60-TMR has a slightly faster H+ decrease). The other reactant (H2BO3) achieves homogeneous mixing first in the baffle configuration, followed by the orifice plate configuration, and TMR and V60-TMR present similar H2BO3 distribution patterns. As a limiting reactant, the faster the concentration of H+ ions decreases, the more H+ ions participate in Reaction R1. Correspondingly, the higher the micromixing efficiency, the lower the XS.

Figure 10.

Figure 10

Component concentration contours under different enhanced structures at Re = 1600: (a) TMR; (b) B-TMR; (c) O-TMR; (d) V60-TMR; (left): H+; (right): H2BO3.

Figure 11 shows the effect of Re on the XS of four TMRs. For all structures, XS decreases with increasing Re (higher turbulence intensity improves mixing). At the same Re, XS follows the order B-TMR < O-TMR < V60-TMR < TMR, indicating that the baffle structure has the best micromixing efficiency, followed by the orifice-plate structure. The baffle structure demonstrates high micromixing efficiency, which is consistent with previous studies on flow perturbation-enhanced mixing [24,26]. However, its significant pressure drop (increasing rapidly with flow rate) limits practical applicability in energy-sensitive systems. The orifice-plate structure offers moderate micromixing performance but still suffers from substantial pressure drop, attributed to sudden flow contraction and separation [34]. In contrast, the venturi structure achieves improved micromixing efficiency with minimal pressure drop increase, making it superior to the conventional TMR for industrial applications. This is because the gradual contraction–expansion design of the venturi guides fluid flow without severe boundary layer separation, reducing energy loss while enhancing turbulence [35]. Therefore, numerical simulations were conducted on microreactors with venturi structures of varying angles, and the effects of geometric angles on their hydrodynamic characteristics (e.g., pressure drop, flow field distribution) and micromixing efficiency were discussed in detail below.

Figure 11.

Figure 11

Effect of Re on XS (different enhanced structures).

Notably, compared with TMR, the venturi structure improves micromixing efficiency (lower XS) with a minimal increase in pressure drop, and no obvious flow dead zones are observed in Figure 7d, making it more promising for practical applications.

3.4. Fluid Dynamics and Micromixing Efficiency of Venturi-Type Microreactors

Figure 12 shows the velocity distribution of venturi-type microreactors (V30-TMR, V45-TMR, V60-TMR, V75-TMR) at Re = 1600. Due to the uniform contraction port size (0.6 mm), all structures show similar velocity distribution patterns, with maximum velocities in the order: V30-TMR > V45-TMR > V60-TMR > V75-TMR. Furthermore, it can also be observed from this figure that, under operating conditions, prominent flow dead zones occur on both sides of the confluence region in the V75-TMR compared with other venturi structures.

Figure 12.

Figure 12

Velocity contour maps of venturi-type microreactors (different contraction angles): (a) V30-TMR; (b) V45-TMR; (c) V60-TMR; (d) V75-TMR.

Figure 13 shows the distribution of turbulent kinetic energy and turbulent dissipation rate along the tube length at Re = 1600. Peaks of both parameters occur within the first 2 mm of the mixing channel (highest turbulence intensity after fluid collision) and gradually stabilize along the tube length. The turbulent kinetic energy peaks follow the order: V30-TMR > V45-TMR > V75-TMR > V60-TMR, while the dissipation rate peaks follow: V30-TMR > V45-TMR > V75-TMR > V60-TMR. Figure 14 presents the velocity and vorticity contours of the mixing zones in the V60-TMR and V75-TMR. Compared with venturi microreactors with a 60° contraction angles, the more gradual 75° contraction angle results in an increased length of the contraction section in the reactor and intensifies boundary layer separation on both sides of the flow channel, consequently leading to a higher maximum turbulent kinetic energy and energy dissipation rate in this region than that of the V60-TMR.

Figure 13.

Figure 13

Distributions of (a) turbulent kinetic energy and (b) turbulent dissipation rate along the tube length (venturi-type microreactors) at Re = 1600.

Figure 14.

Figure 14

Local velocity and vorticity diagrams of venturi-type microreactor at Re = 1600; (a) V60-TMR; (b) V75-TMR; (left): velocity; (right): vorticity.

Figure 15 shows the variation in H+ concentration along the tube length in four venturi-type microreactors with different contraction angles at Re = 1600. As can be observed from the figure, H+ is full consumed at the 12 mm position of the mixing channel, indicating that the reaction process is almost completed here. Furthermore, the smaller the contraction angle, the higher the turbulence intensity after fluid confluence; enhanced mixing thereby accelerates H+ consumption, resulting in a more pronounced decreasing trend of its concentration.

Figure 15.

Figure 15

Variation in H+ concentration along the tube length (venturi-type microreactors) at Re = 1600.

Figure 16 shows the effect of Re on pressure drop and XS for venturi-type microreactors and TMR. It can be seen from Figure 16a that the pressure drop increases with the rise in Re. At low Re conditions, the pressure drops of the several microreactors show little difference. As Re increases, the pressure drop of V30-TMRs is significantly higher than that of the other microreactors, and the higher the Re, the greater the magnitude of this increase. In particular, at higher Re, the pressure drop of V75-TMRs is slightly higher than that of V60-TMR. The XS decreases with the increase in Re in Figure 16b. In the lower Re range, the XS follows the order: V30-TMR < V45-TMR < V60-TMR < V75-TMR. As Re increases, the XS of V75-TMRs decreases more rapidly and gradually approaches that of V60-TMR. In general, smaller contraction angles improve micromixing efficiency but increase pressure drop. However, the turbulence intensity and micromixing efficiency of V75-TMRs with a gentler contraction angle are more sensitive to changes in Re. Under the operating conditions used in this study, the V45-TMRs achieve a balance between energy consumption and mixing efficiency, thus qualifying as the preferable options among venturi configurations.

Figure 16.

Figure 16

Effect of Re on (a) pressure drop and (b) XS (venturi-type microreactors and TMR).

3.5. Micromixing Time

To better carry out a comparative analysis of the micromixing performance among various types of reactors, the agglomeration model was used to estimate the micromixing time (tm) of microreactors with different structures in this study. The model equations are as follows:

dcidt=(cj,A0cj)1gdgdt+rj (17)
g(t)=exp(t/tm) (18)

where cj is the concentration of component j in the mixed stream; cj,A0 is the initial concentration of component j before mixing; rj is the generation rate of component j; and g is the growth rate.

Figure 17 shows the relationship between XS and tm. The tm values of all structures range from 0.025 ms to 0.234 ms. As shown in Figure 18, the B-TMR exhibits the shortest tm among all structures, with a minimum tm approximately 53% lower than that of TMRs under the same conditions. Among venturi-type microreactors, the V30-TMR has the shortest tm, with a minimum tm approximately 35% lower than that of the TMR under the same conditions. These results indicate that structural modifications and contraction angle adjustments reduce tm.

Figure 17.

Figure 17

Relationship between XS and tm.

Figure 18.

Figure 18

Comparison of tm for microreactors with different structures.

As shown in Table 4, the tm calculated in this study are compared with those obtained from other milli/microreactors [48,49]. Factors affecting the tm include the experimental system, intensification measures of the milli/microreactor, operating conditions, and so on. As can be seen from the table, these tm are of a similar order of magnitude to those calculated by Gu [50] because both work systems were operated at relatively high Re. The key influencing factors of the tm in microreactors can be categorized into three types: reactor structural parameters, operational parameters, and physical property parameters of the system. In practical applications, the balance between micromixing performance and energy consumption is achieved through structural optimization and operational regulation, with the goal of obtaining a higher micromixing rate at a lower energy cost.

Table 4.

Comparison of micromixing characteristic time.

Literature Sources Reactor Micromixing Intensification Method Operational Condition tm
This paper T-type microreactor Baffles, orifice-plate, venturi configuration Re = 600–3400 0.025–0.234 ms
Rahimi [48] T-type microreactor Ultrasound wave Re = 71–638 0.65–9 ms
Gu [50] Micro-impinging stream reactor Micro-impinging Rej = 395–3161 0.02–2.1 ms
Yang [49] Corning AFR Heart-shaped configuration Q = 1–9 mL/min 4–17 ms

4. Conclusions

The structural design of microreactors is one of the important factors for regulating flow field characteristics and enhancing micromixing efficiency. In this study, CFD models were established to simulate the fluid flow and mixing-reaction processes in TMRs with different enhanced structures. The effects of microreactor structures on their hydrodynamic characteristics (e.g., pressure drop, flow field distribution) and micromixing efficiency were investigated under different Re. The main results are as follows:

The standard k-ε model with an extensible wall function shows the best agreement with experimental pressure drop data of the TMR, with errors within 25%. A fitting function for the Am is obtained in the Re range of 600–3400, and the errors between simulated and experimental XS values are within 15%.

The baffle structure generates the highest turbulence intensity and the optimal micromixing efficiency, followed by the orifice-plate structure. However, both structures suffer from significant pressure drops, which rise sharply with increasing flow rate. The venturi structure improves micromixing efficiency which minimizes the increase in pressure drop, demonstrating superior application prospects compared to the conventional TMR. Among venturi structures, the V30-TMR achieves the highest pressure drop and micromixing efficiency; the V75-TMR has more distinct flow dead zones than the V60-TMR; V45-TMRs strike a balance between energy consumption and micromixing efficiency under the operation conditions in this work.

The tm of all structures ranges from 0.025 to 0.234 ms under operational conditions. Structural optimization can shorten the tm, with the baffle structure achieving the most significant reduction (≈53% compared to TMRs). The results can provide a theoretical basis and technical guidance for optimizing the structural design of microreactors in fast reaction systems.

Acknowledgments

The authors acknowledge the technical support from the Fundamental Research Project of China National Nuclear Corporation for this work.

Abbreviations

The following abbreviations are used in this manuscript:

CFD Computational Fluid Dynamics
TMR T-Shaped Microreactor
B-TMR Baffle-Type T-Shaped Microreactor
O-TMR Orifice-Plate-Type T-Shaped Microreactor
V30-TMR Venturi-Type T-Shaped Microreactor (30° Contraction Angle)
V45-TMR Venturi-Type T-Shaped Microreactor (45° Contraction Angle)
V60-TMR Venturi-Type T-Shaped Microreactor (60° Contraction Angle)
V75-TMR Venturi-Type T-Shaped Microreactor (75° Contraction Angle)
PDF Probability Density Function
EDM Eddy Dissipation Model
Am Empirical Constant in EDM
XS Segregation Index
tm Micromixing Time
Re Reynolds Number

Author Contributions

Conceptualization, Y.N. and T.Y.; methodology, Y.N.; software, Y.N.; validation, Y.N., B.W. and R.W.; formal analysis, Y.N.; investigation, Y.N.; resources, T.Y.; data curation, Y.N.; writing—original draft preparation, Y.N.; writing—review and editing, T.Y.; visualization, Y.N.; supervision, T.Y.; project administration, T.Y.; funding acquisition, T.Y. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request.

Conflicts of Interest

The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Funding Statement

This research received no external funding.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.Liu Z.L., Zhang P.F. Application of microreactors in chemical engineering. Chem. Ind. Eng. Prog. 2016;35:10–17. [Google Scholar]
  • 2.Suryawanshi P.L., Gumfekar S.P., Bhanvase B.A., Sonawane S.H., Pimplapure M.S. A review on microreactors: Reactor fabrication, design, and cutting-edge applications. Chem. Eng. Sci. 2018;189:431–448. doi: 10.1016/j.ces.2018.03.026. [DOI] [Google Scholar]
  • 3.Fan W.T., Zhao F., Chen M., Li J., Guo X. An efficient microreactor with continuous serially connected micromixers for the synthesis of superparamagnetic magnetite nanoparticles. Chin. J. Chem. Eng. 2023;59:85–91. doi: 10.1016/j.cjche.2022.12.008. [DOI] [Google Scholar]
  • 4.Song Z.Y., Ju S.H. Micro-reactors for nanomaterial synthesis: Manufacturing techniques, current applications and future prospects. Mater. Sci. Semicond. Process. 2026;203:110246. doi: 10.1016/j.mssp.2025.110246. [DOI] [Google Scholar]
  • 5.Guo S., Cao J.Y., Liu M.Q., Zhan L.-W., Li B.-D. Intensification and kinetic study of trifluoromethylbenzene nitration with mixed acid in the microreactor. Chem. Eng. Process. Process Intensif. 2023;183:109239. doi: 10.1016/j.cep.2022.109239. [DOI] [Google Scholar]
  • 6.Tan X.C., Tang M.J., Liu Y.J., Cheng G., Huang W., Xiao C., Tang Y. Enhanced N-amination of nitrogen-rich compounds in the microreactor: Process intensification and morphology control. Chem. Eng. Sci. 2026;320:122697. doi: 10.1016/j.ces.2025.122697. [DOI] [Google Scholar]
  • 7.Zhao X., Bian F.K., Sun L.Y., Cai L., Li L., Zhao Y. Microfluidic generation of nanomaterials for biomedical applications. Small. 2020;16:1901943. doi: 10.1002/smll.201901943. [DOI] [PubMed] [Google Scholar]
  • 8.Li H., Liu X., Xiao Y., Cao K. One-pot synthesis of 5-norbornene-2,3-dicarboxylic anhydride with high exo/endo ratio in a microreactor under high temperature and appropriate pressure. Chem. Eng. J. 2024;498:155561. doi: 10.1016/j.cej.2024.155561. [DOI] [Google Scholar]
  • 9.Yadav D., Lu X., Ma B.-C., Jing D. Advancements in microreactor technology for hydrogen production via steam reforming: A comprehensive review of numerical studies. J. Power Sources. 2024;596:234090. doi: 10.1016/j.jpowsour.2024.234090. [DOI] [Google Scholar]
  • 10.Yadav D., Lu X., Dansena P., Jing D. Numerical analysis of a helical spiral microevaporator-microreformer system for enhanced methanol conversion and hydrogen production. Chem. Eng. Process.-Process Intensif. 2025;209:110149. doi: 10.1016/j.cep.2024.110149. [DOI] [Google Scholar]
  • 11.Han L.Y., Zhu Y.Q., Pang J., Wang X., Ma S., Han X., Wang K., Zhao W. Synthesis of phospholipid vesicles using an electrokinetic turbulent microreactor. Lab Chip. 2025;25:1959–1967. doi: 10.1039/D4LC00992D. [DOI] [PubMed] [Google Scholar]
  • 12.Peñaranda P.A., Noguera M.J., Florez S.L., Husserl J., Ornelas-Soto N., Cruz J.C., Osma J.F. Treatment of Wastewater, Phenols and Dyes Using Novel Magnetic Torus Microreactors and Laccase Immobilized on Magnetite Nanoparticles. Nanomaterials. 2022;12:1688. doi: 10.3390/nano12101688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Tao Y., Wu K.J., He C.H. Continuous synthesis of boron-doped carbon nitride supported silver nanoparticles in an ultrasound-assisted coiled flow inverter microreactor. J. Flow Chem. 2024;14:177–196. doi: 10.1007/s41981-023-00300-1. [DOI] [Google Scholar]
  • 14.Ammar H., Garnier B., Moctar A.O., Willaime H., Monti F., Peerhossaini H. Thermal analysis of chemical reactions in microchannels using highly sensitive thin-film heat-flux microsensor. Chem. Eng. Sci. 2013;94:150–155. doi: 10.1016/j.ces.2013.02.055. [DOI] [Google Scholar]
  • 15.Gayen B., Manna N.K., Biswas N. Enhanced mixing quality of ring-type electroosmotic micromixer using baffles. Chem. Eng. Process. Process Intensif. 2023;189:109381. doi: 10.1016/j.cep.2023.109381. [DOI] [Google Scholar]
  • 16.Tang S.Y., Sivan V., Petersen P., Zhang W., Morrison P.D., Kalantar-Zadeh K., Mitchell A., Khoshmanesh K. Liquid metal actuator for inducing chaotic advection. Adv. Funct. Mater. 2014;24:5851–5858. doi: 10.1002/adfm.201400689. [DOI] [Google Scholar]
  • 17.Qian S., Bau H.H. Magneto-hydrodynamic stirrer for stationary and moving fluids. Sens. Actuators B Chem. 2005;106:859–870. doi: 10.1016/j.snb.2004.07.011. [DOI] [Google Scholar]
  • 18.Demircali A.A., Yilmaz A., Uvet H. Enhanced Fluid Mixing in Microchannels Using Levitated Magnetic Microrobots: A Numerical Study. Micromachines. 2025;16:52. doi: 10.3390/mi16010052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Jalili H., Raad M., Fallah D.A. Numerical study on the mixing quality of an electroosmotic micromixer under periodic potential. Proc. Inst. Mech. Eng. Part C J. Mech. Eng. Sci. 2020;234:2113–2125. doi: 10.1177/0954406220904089. [DOI] [Google Scholar]
  • 20.Yang L.X., Xu F.S., Chen G.W. Effective mixing in a passive oscillating micromixer with impinging jets. Chem. Eng. J. 2024;489:151329. doi: 10.1016/j.cej.2024.151329. [DOI] [Google Scholar]
  • 21.Li Q.Y., Shan C.Y., Qiao J.J., Wang G., Chen S., Zhao D. Taylor flow-enhanced mass transfer process in curved microchannels. Phys. Fluids. 2025;37:062010. doi: 10.1063/5.0272680. [DOI] [Google Scholar]
  • 22.Li P.R., Shi L.Y., Zhao J.C., Liu B., Yan H., Deng Y., Yin B., Zhou T., Zhu Y. Topology optimization design of a passive two-dimensional micromixer. Chem. Phys. Lett. 2023;821:140445. doi: 10.1016/j.cplett.2023.140445. [DOI] [Google Scholar]
  • 23.Garcia-Cardosa M., Granados-Ortiz F.-J., Ortega-Casanova J. A Review on Additive Manufacturing of Micromixing Devices. Micromachines. 2022;13:73. doi: 10.3390/mi13010073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lai C.G., Shan S.M., Feng S., Chen Y., Zeng J., Song J., Fu L. Numerical investigations on heat transfer enhancement and energy flow distribution for interlayer battery thermal management system using Tesla-valve mini-channel cooling. Energy Convers. Manag. 2023;280:116812. doi: 10.1016/j.enconman.2023.116812. [DOI] [Google Scholar]
  • 25.Yang A.S., Chuang F.C., Chen C.K., Lee M.-H., Chen S.-W., Su T.-L., Yang Y.-C. A high-performance micromixer using three-dimensional Tesla structures for bio-applications. Chem. Eng. J. 2015;263:444–451. doi: 10.1016/j.cej.2014.11.034. [DOI] [Google Scholar]
  • 26.Wu Q., Wang Y., Mei D., Si S. Development of methanol steam reforming microreactor based on stacked wave sheets and copper foam for hydrogen production. Int. J. Hydrogen Energy. 2022;47:6282–6294. doi: 10.1016/j.ijhydene.2021.11.221. [DOI] [Google Scholar]
  • 27.Kumar A., Sarkar S., Manna N.K. Passive mixing of microchannel mixers with staggered and opposed obstacles: A comparative study. Chem. Eng. Commun. 2022;209:1056–1072. [Google Scholar]
  • 28.López R.R., Ocampo I., Sánchez L.-M., Alazzam A., Bergeron K.-F., Camacho-León S., Mounier C., Stiharu I., Nerguizian V. Surface Response Based Modeling of Liposome Characteristics in a Periodic Disturbance Mixer. Micromachines. 2020;11:235. doi: 10.3390/mi11030235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Yan L., Wang S., Cheng Y. Numerical Simulation of Mixing Process in a Splitting-and-Recombination Microreactor. Front. Chem. Eng. 2022;3:803861. doi: 10.3389/fceng.2021.803861. [DOI] [Google Scholar]
  • 30.Villermaux J., Dushman R. A new method for the study of micromixing in chemical reactors. Chem. Eng. Sci. 1994;49:5137–5144. [Google Scholar]
  • 31.Abiev R.S., Makusheva I.V., Mironova A.I. Comparison of hydrodynamics and micromixing quality in a two-stage microreactor with intensely swirled flows and in a T-mixer. Chem. Eng. Process.-Process Intensif. 2024;202:109829. doi: 10.1016/j.cep.2024.109829. [DOI] [Google Scholar]
  • 32.Shi X., Xiang Y., Wen L.X., Chen J.-F. CFD analysis of flow patterns and micromixing efficiency in a Y-type microchannel reactor. Ind. Eng. Chem. Res. 2012;51:13944–13952. doi: 10.1021/ie300985q. [DOI] [Google Scholar]
  • 33.Liu Z.D., Lu Y.C., Wang J.W., Luo G.S. Mixing characterization and scaling-up analysis of asymmetrical T-shaped micromixer: Experiment and CFD simulation. Chem. Eng. J. 2012;181:597–606. [Google Scholar]
  • 34.Soleymani A., Kolehmainen E., Turunen I. Numerical and experimental investigations of liquid mixing in T-type micromixers. Chem. Eng. J. 2008;135:S219–S228. doi: 10.1016/j.cej.2007.07.048. [DOI] [Google Scholar]
  • 35.Aoki N., Umei R., Yoshida A., Mae K. Design method for micromixers considering influence of channel confluence and bend on diffusion length. Chem. Eng. J. 2011;167:643–650. doi: 10.1016/j.cej.2010.08.084. [DOI] [Google Scholar]
  • 36.Ouyang Y., Xiang Y., Zou H., Chu G., Chen J. Flow characteristics and micromixing modeling in a microporous tube-in-tube microchannel reactor by CFD. Chem. Eng. J. 2017;321:533–545. doi: 10.1016/j.cej.2017.03.151. [DOI] [Google Scholar]
  • 37.Dong B., Guo Y., Yang J., Yang X., Wang L., Huang D. Turbulence induced shear controllable synthesis of nano FePO4 irregularly-shaped particles in a counter impinging jet flow T-junction reactor assisted by ultrasound irradiation. Ultrason. Sonochemistry. 2023;99:106590. doi: 10.1016/j.ultsonch.2023.106590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Mariotti A., Antognoli M., Galletti C., Mauri R., Salvetti M.V., Brunazzi E. A Study on the Effect of Flow Unsteadiness on the Yield of a Chemical Reaction in a T Micro-Reactor. Micromachines. 2021;12:242. doi: 10.3390/mi12030242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Fournier M.C., Falk L., Villermaux J. A new parallel competing reaction system for assessing micromixing efficiency—Experimental approach. Chem. Eng. Sci. 1996;51:5053–5064. doi: 10.1016/0009-2509(96)00270-9. [DOI] [Google Scholar]
  • 40.Guichardon P., Falk L. Characterisation of micromixing efficiency by the iodide–iodate reaction system. Part I: Experimental procedure. Chem. Eng. Sci. 2000;55:4233–4243. doi: 10.1016/S0009-2509(00)00068-3. [DOI] [Google Scholar]
  • 41.Commenge J.M., Falk L. Villermaux–Dushman protocol for experimental characterization of micromixers. Chem. Eng. Process. Process Intensif. 2011;50:979–990. doi: 10.1016/j.cep.2011.06.006. [DOI] [Google Scholar]
  • 42.Kölbl A., Kraut M., Schubert K. The iodide iodate method to characterize microstructured mixing devices. AIChE J. 2008;54:639–645. doi: 10.1002/aic.11408. [DOI] [Google Scholar]
  • 43.Liu Z., Guo L., Huang T., Wen L., Chen J. Experimental and CFD studies on the intensified micromixing performance of micro-impinging stream reactors built from commercial T-junctions. Chem. Eng. Sci. 2014;119:124–133. doi: 10.1016/j.ces.2014.07.061. [DOI] [Google Scholar]
  • 44.Bourne J.R. Comments on the iodide/iodate method for characterising micromixing. Chem. Eng. J. 2008;140:638–641. doi: 10.1016/j.cej.2008.01.031. [DOI] [Google Scholar]
  • 45.Kölbl A., Kraut M., Dittmeyer R. Kinetic investigation of the Dushman reaction at concentrations relevant to mixing studies in microstructured cyclone type mixers. Chem. Eng. Sci. 2013;101:454–460. doi: 10.1016/j.ces.2013.07.008. [DOI] [Google Scholar]
  • 46.Guichardon P., Falk L., Villermaux J. Characterisation of micromixing efficiency by the iodide–iodate reaction system. Part II: Kinetic study. Chem. Eng. Sci. 2000;55:4245–4253. doi: 10.1016/S0009-2509(00)00069-5. [DOI] [Google Scholar]
  • 47.Song Z.Y., Zhang Y.X., Chu G.W., Shao L., Xiang Y. Micromixing efficiency and enhancement methods for non-Newtonian fluids in millimeter channel reactors. Chin. J. Chem. Eng. 2025;78:108–119. doi: 10.1016/j.cjche.2024.08.006. [DOI] [Google Scholar]
  • 48.Rahimi M., Aghel B., Hatamifar B., Akbari M., Alsairafi A.A. CFD modeling of mixing intensification assisted with ultrasound wave in a T-type microreactor. Chem. Eng. Process. Process Intensif. 2014;86:36–46. doi: 10.1016/j.cep.2014.10.006. [DOI] [Google Scholar]
  • 49.Yang M., Yang L.N., Zheng J., Hondow N., Bourne R.A., Bailey T., Irons G., Sutherland E., Lavric D., Wu K.-J. Mixing performance and continuous production of nanomaterials in an advanced-flow reactor. Chem. Eng. J. 2021;412:128565. doi: 10.1016/j.cej.2021.128565. [DOI] [Google Scholar]
  • 50.Gu R.J., Cheng K.P., Wen L.X. Application of the engulfment model in assessing micromixing time of a micro-impinging stream reactor based on the determination of impinging zone with CFD. Chem. Eng. J. 2021;409:128248. doi: 10.1016/j.cej.2020.128248. [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data presented in this study are available on request.


Articles from Micromachines are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES