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Manufacturing of Mycelium-Based Biocomposites: Conference Paper
Manufacturing of Mycelium-Based Biocomposites: Conference Paper
Manufacturing of Mycelium-Based Biocomposites: Conference Paper
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1. INTRODUCTION
Almost all plastic materials used today are made with little regards to sustainable
end-of-life options. When plastic resins are combined with reinforcement fibers such as
glass or carbon, and low-density cores such as foam or honeycomb to make advanced
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composite parts and sandwich structures with composite skins, their end-of-life options
are even worse. This situation has led to worldwide concerns over the environmental
issues related to the disposal of non-biodegradable plastic and polymer composite
materials after their intended use. The idea of developing biodegradable materials that
have similar performance to traditional engineering materials, but will undergo a
complete but controlled biodegradation just like any other organic waste, has been of
interest to researchers for many years, although most of the current research and
applications have focused on reinforcements [1-3]. Some examples of prior R&D
include:
Henry Ford, in the 1930s and 1940s, mixing soy protein with
phenol-formaldehyde resin to produce automobile body parts [4]
Brother and McKinney reportedly making plastics using soy protein and various
cross-linking agents [5]
Drzal et al. finding the combination of bio-fibers like kenaf, hemp, flax, jute,
henequen, pineapple leaf fiber and sisal with polymer matrices can be used in
automotive applications [6] and
Flanigan et al. using natural fibers to replace either part or all of the glass fiber
reinforcement used in the composites in order to increase the bio-content [7].
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„mycocomposite‟ materials made using natural fibers such as kenaf, jute, hemp, flax,
bamboo, and sisal over traditional synthetic composites are low cost, low density,
competitive strength, tensile and impact mechanical properties, reduced energy
consumption, the potential for CO2 sequesterization, and perhaps most important of all,
biodegradability [6]. The low-embodied-energy production process used for
mycocomposites makes them cost competitive with synthetics, but the material is
inherently sustainable since it will biodegrade under the proper conditions or can be
recycled into feedstock for packaging or composite core material; thus diverting waste
from landfills. Mycocomposites are inherently safe – the material is stable when exposed
to high temperatures (200-400C ignition point range) or ultraviolet radiation, and the use
of vegetative tissue prevents the formation of spores, a potential allergen and friable
particle if made inactive (i.e. killed) by heating within a certain time period. The
bio-based core and reinforcement can offer enhanced structural and thermal performance,
while the mycelium acts as a binder, shown in Figure 2, similar to the role of a polymer
resin matrix. A typical cycle time is about 5-7 days, as previously mentioned, to
adequately colonize the reinforcement fibers and/or core material, and longer
colonization leads to stiffer and stronger final products. A smoother surface can also be
achieved through full colonization.
(a) (b)
Figure 1: (a) Schematic and (b) picture of mycelium-based composites or
„mycocomposites‟
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Figure 2: SEM image of mycelium hyphae growing on a natural fiber
In parallel with the material development effort at Ecovative, the Rensselaer CATS
has been focusing on full-scale production of long fiber mycocomposites. Small batch
production of such material has already been done commercially by hand lay-up at
Ecovative [9], while the CATS has begun investigating various manufacturing processes,
particularly for the laminate skins, for manufacturing scale-up. This paper discusses
Rensselaer‟s current research related to this scale-up effort for sandwich composites.
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curing processes. This has made the cost of producing biocomposites parts remain high,
and thus limiting its extensive use in vast applications.
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recording the number of uncut threads, numbers of frayed threads, and cutting accuracy
on a 1-10 relative scale.
(a) (b)
(c)
(d)
Figure 3: (a) Shoe-shaped woven jute composite ply, (b) curtain-coating of an individual
ply with natural glue, (c) forming of 2-ply stack with matched molds, and (d) drying the
skins using simple heated platens.
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3.2 Ply Impregnation with Natural Glue
Several methods were investigated for impregnating individual plies (woven jute)
with a natural glue that is compatible with mycelium growth including dip-and-soak,
spray coating, and curtain coating (shown in Figure 3(b)). For the-dip and-soak process,
two different ways were tested: dry and wet. The dry method involves putting the pre-cut
sample into the glue directly, while the wet method involves pre-wetting the sample with
water and then continuing with the dip-and-soak. For the spray coating process, a
commercially available spray gun designed for automotive painting was used, and two
different spray flow rates (corresponding to 20 psi and 30 psi input pressures) were tested.
For curtain coating, a converted fish tank waterfall filter was used. The authors found that
the contact time between the glue „waterfall‟ and the sample can be very short compared
with other impregnating methods, even though it had to be sent through twice to cover
both sides. Process outputs measured include dip time, spray pressure, sample starting
weight and wet weight, coating time, and impregnation coverage.
The natural glue used in all tests consisted of water, starch and maltodextrin. Starch
can be heat activated to create strong bonds for holding together pre-forms, but the
problem of syneresis requires the solution to be constantly mixed. Maltodextrin helps to
increase viscosity.
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laminate. A wooden male mold and thermoformed plastic female mold in the shape
of a shoe sole were used to pre-form two-ply thick specimens.
The DDF process was investigated using an existing machine available in the CATS.
DDF typically involves: sandwiching an uncured stack of reinforcement (e.g., cloth)
pre-impregnated with resin (called „pre-preg‟) between two silicone diaphragms
evacuated in between and suspending over a rigid frame; heating the pre-preg stack
(typically with a blanket heater) to lower viscosity resin; and pulling the stack down
over a rigid, stationary mold using differential pressure. Vacuum pressure on the
diaphragms helps prevent buckling of the laminate during formation. After the
vacuum between the diaphragms is released and the top diaphragm is lifted, the
pre-formed skin or core is quickly frozen or dried (mycelium can survive either
condition) to retain its formed shape and then be placed in another mold for
drying/sterilization.
Process outputs measured for these forming processes include cycle time (time required
for the forming process), glue contact time (time that a worker will be physically in
contact with the glue), degree of wrinkling, and quality on a 1-10 relative scale.
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entire drying process, and energy usage measured using a P3 international P4400
Kill-A-Watt electricity usage monitor. Compliance, strength, and heating quality were
also recorded for the drying quality.
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The ranking matrix for ply impregnation with natural glue is shown by Table 2. It
should be mentioned that the cost of glue is the average unit price multiplied by the
average glue usage. Based on the weighted totals, the dip & soak and curtain coating
methods are preferable to all other impregnation methods.
The ranking matrix for forming laminate skins is shown in Table 3. The DDF process
was immediately eliminated from consideration, because it simply was not suited for the
relatively messy „glued‟ materials or for the low cycle times envisioned for production.
With regards to ranking metrics, “Inferiority” is used instead of quality, since the ranking
required „smaller is preferable‟ metrics. Based on the ranking, match mold forming is the
clear choice for high production.
Table 3: Ranking matrix for forming laminate skins
Stacking Degree of Inferiority
Cycle time Contact time
Processes Wrinkling (1/quality)
Weighted
Units min seconds 0-10 >0.1
Total
Weighting
*10/8 *8/65 *8/5 *8/0.167
(1-10)
Hand layup 8 65 5 0.167 34
Match mold
1 20 1 0.111 10.63
stamping
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The ranking matrix for skin drying is shown in Table 4. The strength of the samples
is converted to peel weakness for statistical purposes. The strength of the sample is
defined as the maximum force required to separate two 2.5 cm-wide plies glued together.
And the peel weakness is the reciprocal, namely 2.5 cm width divided by the maximum
forces to separate two plies. The compliance of the samples is the displacement of a 2.5
cm-wide cut sample in three-point bending experiment with an 8-cm span length and
subjected to a 292 g weight. The overall drying quality is measured on a relative scale
between -10 and 10, where a negative number means under-heated and white (signifying
starch did not fully activate), a positive number stands for overheated and burnt, and 0
signifies an optimal glued condition. Absolute values are used in the comparison, since
negative numbers would not work for the weighted process output summation. After
comparison, the authors concluded that low powered microwave drying and flipped
sample method are of relatively low total number and were selected for further
investigation.
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Convection
12.999 4.608 5.1 2.78E+05 2.5 0.511 |1| 16.4
Oven
Heated Tool 11.7625 3.9775 10 4.85E+05 3 1.969 |0| 16.6
Infrared
11.645 4.07 20 2.93E+05 10 7.353 |-1| 26.4
light
Heated tool
12.014 3.881 5.892 3.72E+05 2 0.564 |-2.5| 20.8
& Infrared
Heated tool
& Infrared 12.459 4.442 6.65 4.20E+05 2 0.912 |0.25| 15.6
(flipped)
~0.5
Air dry 11.2325 4.8375 0.00E+00 7 9.259 |-3| 38.5
day=720
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Figure 4: Proposed layout of manufacturing system concept
REFERENCES
1. Fowler, Paul A, J Mark Hughes, and Robert M Elias. "Biocomposites from crop
fibres and resins." IGER INNOVATIONS. 2007: 66-68. Web. 13 Jan. 2013.
<http://www.aber.ac.uk/en/media/fowlerhugheselias.pdf>.
2. Mohanty, A. K., M. Misra, and L.T. Drzal. "Sustainable Bio-Composites from
Renewable Resources: Opportunities and Challenges in the Green Materials
World." Journal of Polymers and the Environment. 10.1/2 (2002): 19-26. Web. 13
Jan. 2013.
3. SAHEB, D. NABI, and J.P. JOG. "Natural Fiber Polymer Composites: A
Review." Advances in Polymer Technology. 18.4 (1999): 351-63. Web. 13 Jan.
2013.
4. William F. Powers, “Automotive Materials in the 21st Century”, Adv. Mater.
Process, May 2000, p. 38-41.
5. G. H. Brother and L. L. McKinney (1940) Ind. Eng. Chem. 32, 1002.
6. Drzal, Lawrence T., A.K. Mohanty, and M. Misra. "BIO-COMPOSITE
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MATERIALS AS ALTERNATIVES TO PETROLEUM-BASED COMPOSITES
FOR AUTOMOTIVE APPLICATIONS." 2001 SPE ACCE PROCEEDINGS Web.
13 Jan. 2013. <http://speautomotive.com/SPEA_CD/SPEA2001/pdf/e/E1.pdf>.
7. Flanigan, Cynthia, Christine Perry, Ellen Lee, Dan Houston, Debbie Mielewski,
and Angela Harris. “Use of agriculture materials in flexible polyurethanes and
composites for automotive applications.” 2006 SPE ACCE PROCEEDINGS Web.
13 Jan. 2013.
<http://speautomotive.com/SPEA_CD/SPEA2006/PDF/c/c3.pdf>.
8. "Our Technology." Ecovative. N.p.. Web. 25 Mar. 2013.
<http://www.ecovativedesign.com/about-our-materials/core-tech/>.
9. "About Ecovative." Ecovative. N.p.. Web. 13 Jan. 2013.
<http://www.ecovativedesign.com/about-ecovative/>.
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