3. Results and Discussion
The flow curve confirmed that the dried malted rice test solutions were Newtonian fluids.
The measured range is 103 in the shear rate. The experimental results for the friction factor
λ󠅍 based on the pressure loss data are shown in
Figure 2. It is defined as
. Where, are the pressure loss, the pipe diameter, the density, and mean velocity, respectively. Reynolds number is defined as using the kinematic viscosity ν. The friction factor of tap water matches well with that of Newtonian fluids in the laminar and turbulent flow ranges. Drag reduction occurred for all the test solutions.
Table 2 lists the drag reductions (%). The maximum drag reduction was approximately 27%. In the friction factor vs.
Re plots in
Figure 2, the friction factors of these biopolymer solutions are parallel to and below those of water, which indicates type-B drag reduction [
11,
12]. This phenomenon occurs in partially hydrolyzed polyacrylamide with linear
random-coil-structured macromolecules in solution. Because the reduced friction factors of the test solutions were aligned parallel to those of Newtonian fluids, the drag reduction of the malt-rice solutions was type B.
For solution D, the transition
Re increased compared with that of tap water. Drag reduction in solution B was greater than that in solution A, although the culture temperature and time remained the same (
Table 1). The initial masses of dry malt were 500 and
500g for solutions A. The most divergent solution preparation conditions involved the removal of the solid components after culturing using a filter mesh. The sizes of these meshes were 0.9 and
20m for solutions A and B, respectively. The Aspergillus (5–10
m) was removed with an extremely fine 0.9-μm filter. Solutions C and D contained reduced amounts of dried malted rice and water compared to solutions A and B, respectively. The aqueous test solution with the largest drag reduction was Solution D, which required a shorter culture time than the other solutions. However, the current experimental data cannot be used to determine the culture conditions for a specific drag reduction %.
We determined the relationship between the sugar content (degrees Brix) resulting from the culture process and the culture time.
Figure 3 shows the variations in drag reduction and sugar content with culture time for solutions with other preparation conditions, similar to those of solution D. As shown in
Figure 3, the number of disaccharides produced initially increased with cultivation time, plateaued with a further increase in cultivation time, and then increased again with the cultivation time.
The drag reduction % was maximized in the region where the sugar content remained constant over time during cultivation. Thus, it can be inferred that polysaccharides were produced by the cultivation of Aspergillus oryzae. However, the quantitative relationship between disaccharide content and drag reduction is unknown. The malt-to-water ratios were identical for solutions C and D. However, the drag reduction in solution D is significantly higher than that in solution C. It can be considered that, in solution C, the cultivation of the Aspergillus was in a state of saturation owing to the increased cultivation time.
The friction factor
λ󠅍, based on the pipe pressure difference (
Figure 2), can be used to conveniently calculate the pressure of pipeline systems. However, it is not sufficient to analyze the flow behavior of
a circular pipe. The friction factor
f based on the shear stress
τw acting on the pipe wall was used to obtain the relationship between the friction factor and velocity profile. This relationship is necessary for explaining the onset and mechanism of the drag reduction phenomenon.
Figure 4 shows the friction factor based on the wall shear stress.
As mentioned above, the friction factor f is defined as . In
Figure 4, L (dotted line) and N (solid line) represent the results for the laminar and turbulent flows of Newtonian fluids, respectively, and M (dashed line) is the MDRA obtained by Virk [
13,
14]. The experimental data points diverge from the MDRA at
Re√
f ≅200~
250 and align above and
nearly parallel to N. According to the results,
Re√
f ≅ 200 marks the onset of the drag reduction phenomenon.
In the turbulent flow range, the experimental data points were aligned parallel to those of Newtonian fluids, which indicated type-B drag reduction. To understand flow behavior, it is necessary to analyze the velocity profile. Because the velocity profile in the pipe was not measured in this study, we predicted it using analytical results considering type-B drag reduction.
Virk [
12] defined the flow enhancement during type-B drag reduction as
where
f and
fn are the friction factors of the aqueous test solutions and the Newtonian fluid, respectively. The second term on the right side of Eq. (1) represents the Prandtl–Karman equation:
Because the concentrations of the aqueous test solutions could not be measured in this study, we estimated the concentration of the test solution by comparing it with that of the xanthan gum solution. The results of the test solutions were extrapolated from Virk’s data using
S' obtained from Eq. (1), as shown in
Figure 5. Solutions D and
Cw=50-ppm xanthan-gum solutions exhibited equivalent drag reduction characteristics.
The mean velocity in the pipe flow must be determined to determine the drag-reduction mechanism. Watanabe and Ogata [
15] derived an equation to predict the mean velocity by
S'.
The mean velocity profile for a fully developed turbulent flow through a smooth pipe is
where
and
.
ū is the mean velocity over time and
is the friction velocity (
), where
τw and
ρ are the shear stress and density, respectively. The parameter
y is the distance measured from the wall,
y = (
ɑ –
r), where
ɑ is
inner pipe radius.
Using an example from the experimental results for the friction factor of aqueous dried malted-rice solutions in regions of turbulent flow, we assumed that the velocity profile is expressed by Eq. (2).
The friction factor is calculated by
For Newtonian fluids, we set
κ and
C equal to 0.4 and 5.5, respectively. Thus, Eq. (3) becomes
The constant 0.6 in Eq. (4) must be modified so that the flow characteristics agree with the experimental data. Hence, we modified Eq. (3) to
If ζ = 2/3, κ = 0.4, and C = 5.5 are substituted into Eq. (5), we obtain the Prandtl–Karman formula:
Because the friction factor of the suspensions decreased parallel to those obtained using the Prandtl–Karman formula, as shown in
Figure 3, it is reasonable to fix
κ as a constant of 0.4. The substitution of Eq. (5) into Eq. (1) and modifying the constant value to fit that of Newtonian fluids when
S' = 0 yields
Equation (6) enables prediction of the friction factors of Newtonian fluids. Finally, we estimated the mean velocity profile of the pipe flows of aqueous dried malted-rice solutions using C from Eq. (6), if the value of S' is obtained from experimental data using the friction factor.
For example, using the experimental values of
S' = 0.3 and
S' = 2.4, for solutions A and D from
Figure 3, the velocity profile was estimated as
Figure 6 shows the predicted velocity profiles. The viscous layer thickens in the region where the drag reduction occurs. Because the predicted velocity distribution shifts upward with increasing drag reduction rate, the thickness of the viscous layer increases.
Japper-Jaafar et al. [
15] experimentally investigated the drag reduction in a fully developed turbulent pipe flow of an aqueous solution of a rigid “rod-like” polymer, scleroglucan, at concentrations of 0.005% and 0.01% (similar to type-B drag reduction). Mean velocity profiles and turbulent fluctuation levels were measured using a laser Doppler anemometer. The experimental friction factor curves were parallel to those of Newtonian fluids, and the experimental friction factors were lower than those of Newtonian fluids. This finding is qualitatively consistent with the results of this study.
Meanwhile, prediction of the drag reduction ratio of diluted solutions will be convenient for the actual application of this biopolymer solution.
Figure 7 depicts the effect of the drag reduction of the diluted solution. The test solution was cultured under the same conditions as Solution D in
Table 1. In the experiment, the stock solution was diluted twice and four times with water and the drag reduction ratio was measured at Re = 3410~3610. As a result, the maximum drag reduction ratio was 8.3% at Re = 6x10
3. The solid line in the figure is given by
, here
is a concentration regarding 100% as 1. The results are in agreement with the experimental data, with the errors of 11% and 15% at
=50% and 25%, respectively. Therefore, if the drag reduction ratio of the stock solution is known, the drag reduction ratio of the diluted solution can be predicted from
within a 15% error range.
The physical properties of polymer solutions degrade depending on external changes. Mechanical shear degradation is particularly problematic, and can hamper the practical application of polymer solutions for turbulent drag reduction phenomena. Mechanical degradation refers to the chemical process in which the activation energy of polymer chain scission is exceeded by the mechanical action on the polymer chain, and bond rupture occurs. Many corresponding experiments have been performed under turbulent flow conditions using various experimental apparatus. We examined the mechanical degradation of test solutions experimentally. In this study, a discharge pipeline system [
14] was employed to measure the pressure loss relative to the mechanical degradation. The system comprises a syringe-type pump and a syringe directed into a test pipe. The test solution is fed into the syringe and the pressure loss is measured repeatedly. The results are presented in
Figure 8. From
Figure 7, the drag reduction ratio clearly decreases after two to three repetitions and then asymptotically approached a constant value. However, the drag reduction phenomenon disappears in the high-Re range. This is replotted in
Figure 9 for clarity incorporating the experimental data of the friction factor.
Observation of microscopic photographs of the solution in which the drag reduction phenomenon has disappeared, reveal that the size of the conidial spore itself had decreased, and had been cut by the mechanical shearing. From these observation results, it is not possible to clearly determine changes in the molecular bonding state of polysaccharides. It will be necessary to clarify the mechanical degradation of biopolymer, including the effects on the growth of conidia and its modification according to turbulent flow in the future.