2 Feb 2017 Quantitative Evaluation of The
2 Feb 2017 Quantitative Evaluation of The
can withstand temperatures up to 250 C. A 0.8 mm-thick polycar- particles). The sintered-coating fabrication method is adjusted to
bonate plate is attached to the top of the PEEK block; the copper achieve a range of porosities for each particle shape. This requires
block is aligned such that it protrudes just above the polycarbon- either reducing or increasing the native packing density of the
ate plate as shown. The vertical location of the thermocouple rake powder. The porosity of the coating can be reduced by
and the thickness of polycarbonate plate have been slightly altered controlling the sintering time and temperature to achieve the
from the original design [9]. The lower part of the copper block is desired porosity [9]. In order to increase the porosity beyond the
insulated as described in Ref. [9]. native packing density, the most commonly used method is lost-
The pool boiling chamber comprises four polycarbonate walls carbonate sintering (LCS) [29]. A mixture of spherical metal par-
sealed together with RTV silicone that is cured under compression ticles, carbonate, and a binder is sintered at high temperature
with screws. The chamber is sealed to the base heater assembly under pressure until the carbonate decomposes or melts, leaving
with a compressed PTFE gasket. An aluminum cover plate seals behind a porous metal coating. The carbonate particle size and
the top of the chamber walls by compressing another PTFE gas- percentage, as well as the sintering temperature and time, can be
ket, forming a 30.48 mm 30.48 mm 93.9 mm sealed chamber controlled to produce porous coatings with the desired porosity
enclosing the working fluid on the heated surface. A T-type ther- and pore diameter.
mocouple routed through the cover plate is used to measure the The top surface of the copper heater block is prepared for sin-
pool temperature during testing. A chilled 50–50% water–glycol tering by sanding with progressively finer diamond sanding sheets
mixture is cycled through the condenser at a flow rate of 0.5 l/min (9 lm, 3 lm, and 0.1 lm) followed by metal polishing (Simi-
at 15 C using a chiller (ULT-80, Neslab) to condense vapor dur- chrome, Happich, Wuppertal, Germany). The irregular particles
ing testing. A 6.35 mm-diameter polyurethane tube connects the (ACuPowder International) and the spherical particles (Alfa
liquid pool to a vapor trap that is open to the ambient during test- Aesar) are first sieved into the desired size range of 90–106 lm.
ing and maintains the pool at atmospheric pressure. The chiller The range is selected based on the particle size that yielded the
flow rate and set-point temperature were selected to ensure that no best pool boiling heat transfer performance for spherical sintered
working fluid collects in the vapor trap during the experiment (to coatings at 40% porosity in a prior study [9]. The particles are
prevent fluid loss from the chamber over time). cleaned by soaking in acetone and rinsing with methanol. To sin-
ter the porous layers with a reduced porosity, loose copper powder
2.2 Fabrication of Test Surfaces. Copper particles having is first poured into a graphite mold and leveled off to the desired
two different morphologies—irregular and spherical—were used height. The initial layer thickness of particles is varied, as
to fabricate the test surfaces. The differences in morphology are required, to obtain a final layer thickness-to-particle diameter
brought about by the particle fabrication method. As described in ratio, d/d, of 4, which has been shown to have the maximum
Refs. [27,28], irregular particles are produced by water atomiza- heat transfer coefficient in previous studies [7,30]. The copper
tion and spherical particles by air atomization. Irregular particles block is then gently placed face-down on top of the powder and
appear as roughened spheroidal shapes, while spherical particles the assembly is placed in an evacuated furnace. The temperature
are smooth. Figure 2 shows representative images of the particle is steadily ramped up to 950 C and held at this temperature under
shapes observed using a scanning electron microscope (SEM). vacuum for the desired time as shown in Table 1. The assembly is
The SEM images are taken after testing. Due to the different mor- then allowed to gradually cool to room temperature under vacuum
phology of the particles, the native packing porosity before sinter- and inspected under an optical microscope at multiple locations to
ing is different (48% for spherical particles and 60% for irregular ensure a uniform coating thickness.
Fig. 4 Three-dimensional reconstructed solid domain (after thresholding) for (a) spherical
and (b) irregular coatings at a low, intermediate, and high porosity
Particle shape e (%) Domain size x y z (lm lm lm) Number of cells (106)
Kz
U¼ rp (3)
l
variation boundary condition. This boundary condition fixes the where q00 is the heat flux on the bottom wall, @T=@z is the temper-
pressure on the inlet and outlet faces of the domain such that the ature gradient along the z-direction, and kz is the effective thermal
pressure drop per unit length between the inlet and outlet faces is conductivity of the medium along the z-direction.
one unit. Linear pressure variation is imposed across the lateral The physics modules in the software use a finite element-based
faces, which mimics the more conventionally used symmetry homogenization solver. The pressure and velocity components are
boundary condition [32]. These boundary conditions are shown in discretized with continuous linear nodal elements. Further details
Fig. 6(a). The effective permeability in the flow direction (z-direc- about the solution methods and boundary conditions may be found
tion) is obtained using Darcy’s law in Ref. [32].
Fig. 6 Boundary conditions for (a) conduction through copper and pore domains and (b)
flow through the pore domain, used to obtain the effective conductivity and effective perme-
ability, respectively
Particle shape e (%) dpore (lm) dpart (lm) / Sint (mm1) Sneck (mm1) Kz (105 mm2) kz (W/m K) hav (kW/m2 K) CHF (kW/m2)
Fig. 9 Representative contours of (a) pressure field in the pore domain, (b) temperature field
in the solid domain, and (c) temperature field in the pore domain for the spherical particle
coating at 39% porosity. The corresponding contours for irregular particle coatings at 66%
porosity are shown in (d–f). The contours are obtained from numerical simulation of the effec-
tive permeability and effective thermal conductivity.
is merely an indicative representation of the heat transfer coeffi- 50 lm to 100 lm over the porosity rage), as was observed
cient provided by the coating across much of the boiling curve. qualitatively from the SEM images. The average pore size (as
It may be noted here that while all coatings were fabricated well as the standard deviation) shows a gradual increase with
using loose particles sieved to the same size range (90–106 lm), porosity up to an intermediate value (55% for spherical and 58%
the average particle diameters are reduced upon sintering, and are for irregular particle coatings), followed by a sharp increase. This
observed to be of the same order, of 70–85 lm. The sphericity quantitative characterization is consistent with the drastic change
of the coatings is also observed to be fairly constant over the range in the trends of the boiling heat transfer coefficient and CHF noted
of porosities investigated. The irregular particle coatings show a at this intermediate porosity, as was described in Sec. 4.1. This
slightly smaller average sphericity compared to the spherical par- sharp increase may be attributed to the large increase in the per-
ticle coatings. The sphericity is indicative of the qualitative mor- centage of carbonate particles from 10% to 45% that was neces-
phological differences between the two types of coatings formed sary to achieve the desired higher porosity. While for low
by spherical and irregular particles. carbonate percentages (0–10%), the pore size may be dominated
For both spherical and irregular coatings, the average pore by the size of copper particles, the pores formed at higher carbon-
diameter increases with an increase in the coating porosity (from ate percentages may be determined by both the carbonate and the
copper particle sizes, and hence show a wider size distribution. general trends of the boiling performance, it is insufficient to
Coatings with higher porosity and pore sizes are also shown to explain the finer differences such as the drastic change in CHF,
have higher permeability values in Table 3. Since permeability which is more clearly explained from the pore structure analysis.
indicates the ease with which fluid can pass through the coating, Hence, a high-fidelity characterization of the pore statistics is
higher permeability leads to more efficient vapor escape, resulting essential to interpreting the boiling performance of the coatings,
in a higher CHF. This is in accordance with the observations as is performed herein.
above, where coatings with a higher porosity or pore size show a The unit interfacial area (Sint) of the sintered particle coatings
drastic increase in CHF due to the associated higher permeability. denotes the surface area available for heat transfer between the
Irregular particle coatings which have smaller pore sizes also have solid and fluid domains during boiling, while the unit necking area
lower permeability, and hence, lower CHF than spherical particle (Sneck) indicates the contact area available for solid–solid conduc-
coatings at similar porosity. While measuring the bulk coating tion between individual copper particles. For both spherical and
characteristics such as porosity may provide insight into the irregular particle coatings, an increase in porosity is associated
Table 5 Analysis of the relationship between the geometric and effective thermophysical properties on boiling performance char-
acteristics. The critical input properties affecting each output are shown underlined and bold.
Average heat Geometric property e f(e) 0.96 0.31 f(e) 0.96 2.6
transfer coefficient, dpore f(dpore) 0.94 0.79 f(dpore) 0.91 7.6
hav (kW/m2 K) Sint f(S2int) 0.92 9.9 f(S2int) 0.92 42.5
Sneck f(Sneck) 0.92 1.5 f(Sneck) 0.98 1.0
dpart f(dpart) 0.56 88.4 f(dpart) 0.87 13.1
rdpore f(rdpore) 0.85 5.3 f(rdpore) 0.90 9.3
/ f(/) 0.21 738 f(/) 0.77 32.4
e, dpore, Sneck f(e, dpore, Sneck) 0.93 39.5 f(e, dpore, Sneck) 0.96 114
Effective thermo- Kz f(Kz) 0.84 6.8 f(Kz) 0.67 56.2
physical property kz f(kz) 0.98 0.13 f(kz) 0.97 1.20
Critical heat flux, Geometric property E f(e) 0.80 10.1 f(e) 0.81 23.6
CHF (kW/m2) dpore f(dpore) 0.80 9.8 f(dpore) 0.85 16.5
Sint f(Sint) 0.95 0.59 f(Sint) 0.88 11.4
Sneck f(Sneck) 0.74 18.2 f(Sneck) 0.71 47.6
dpart f(dpart) 0.58 48.6 f(dpart) 0.75 37.4
rdpore f(rdpore) 0.91 1.9 f(rdpore) 0.81 25
U f(/2) 0.10 539 f(/2) 0.86 71.8
e, dpore, Sint f(e, dpore, Sint) 0.99 2.4 f(e, dpore, Sint) 0.99 55.6
Effective thermo- Kz f(Kz2) 0.93 8.8 f(Kz2) 0.91 46
physical property kz f(kz) 0.79 10.8 f(kz) 0.70 49.2