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. 2021 Nov 25;5(3):873–921. doi: 10.1007/s42247-021-00319-x

Table 4.

Morphology, density, mechanical performance, water related, and other interesting properties of some recent developments on bio-based biocomposite foams

Bioplastic Filler and concentration Treatments and coatings Processing technology Thickness (mm) Density (g cm−3) Cell size and density Mechanical properties Moisture content and water sorption Other interesting properties References
Glyoxal cross-linked cornstarch Corn husk fiber and kaolin (0 and 10%wt dry starch basis) Beeswax coating Gelatinization and thermoforming 3.38–3.87 0.27–0.31 300–600 μm for only starch foam and 750–900 μm for beeswax foams

Flexion test

σma = 3.2–4.49 MPa

εBb = 4.79–5.30%

Ec = 134.2–109.6 MPa

9.64–10.31%

0.1–0.45 g water/gDB

(both decrease with filler and coating)

The addition of kaolin, fiber, or beeswax appears to enhance the foaming ability of the trays [402]
Cassava starch Kaolin (3, 6, 9, 12, and15%wt) - Compression thermoforming 4 0.21–0.29 370–810 μm (increase with filler content)

Impact test

Maximum strength = 246.1–1151.6 J m−2

Water sorption 9.79% for 3% kaolin foams at RH of 55% Kaolin increase foams impact strength and density with kaolin content [403]
Cassava starch Malt bagasse (0 to 20%wt of solids) - Compression thermoforming 2.16 − 2.24 0.415 − 0.450 -

Tensile test

σma = 10.37–12.92 MPa

εBb = 1.1–1.8%

(at 58% RH)

0.18–0.21 g water/gDB

(decreases with filler)

- [106]
Cassava starch

Sesame cake (SC)

(0 to 40%wt of solids)

- Compression thermoforming 3.3–4.6 0.23–0.30 (filler addition decrease density) -

Tensile test

σma = 0.43–1.16 MPa

εBb = 2.0–3.3%

Ec = 17.8–40.4 MPa

Flexion test

σma = 1.9–7.4 MPa

εBb = 1.1–1.4%

Ec = 174–522 MPa

Water sorption capacity 141–154% (decreases with residue content)  > 20% SC biocomposite foams resulted in most mechanical properties comparable to commercial EPS [21]
Cassava starch Shrimp shell (SH) and egg shell (EG) (0 to 20%wt) - Compression thermoforming 4 0.206–0.286 (increased by SH and decreased by EG) Not reported, SH foams show denser structure and EG foams a more expanded one

Impact test

Maximum strength = 144.18 J/m2 (5% SH) and 171.18 J/m2 (15% EG)

- The izod impact strength of EG starch based reinforced foams increased in 300% [362]
Cassava starch Grape stalk (0–7%wt) - Compression thermoforming 3 0.18–0.21 (filler decrease foam density) Composite foams present a sandwich-type structure

Flexion test

σma = 2.5–2.9 MPa

εBb = 1.3–1.9%

Ec = 150–202 MPa (no significant differences between 0 and 7% filler content)

2.8–8.5% (increases with filler addition) The more expanded structure of biocomposite foams favored biodegradation kinetics [390]
Cassava starch Peanut skin (0–24%wt of solids) - Compression thermoforming 3 0.21–0.27 -

Tensile test

σma = 1.0–1.1 MPa

εBb = 3.9–4.9%

Ec = 25–26 MPa

9.0–9.7% (lower with filler addition) Biocomposite show rougher surface with some holes, but with reduced hydrophilicity [359]
Cassava starch Macroalgae (H. macrolaba) (0 to 20%wt dry starch basis) - Compression thermoforming 4 0.16–0.27 Biocomposite foams present smaller cell-size, higher cell density and thicker cell wall

Impact test

Maximum strength = 33–45 J/m2

- Thermal stability of the foam was improved with filler addition [404]
Cassava starch Water hyacinth (WH) (0, 3, 5, 7, or 10%wt dry starch basis) Beeswax coating Compression thermoforming 4 0.320–0.433 440–560 μm (filler decreases cell size and increases cell density)

Flexion test

σma = 2.95–3.42 MPa

εBb = 3.09–3.52%

Ec = 93–232 MPa

6.77–10% (lower value for 5%wt of WH) Beeswax coating reduced water solubility over a 50% [364]
Cassava starch Sunflower oil cake (SOC) (0 to 40%wt of solids) - Compression thermoforming 3 0.20–0.40 (increases with filler content) 169–278 μm (decreases with filler content)

Flexion test

σma = 3.18–6.26 MPa

Compression test

Hd = 3.91–21.69 kgf

Ene = 31.2–118.2 mJ

12.3–12.8%

40.4–46.9 g water/gDB

Biocomposite foams show greater biodegradability [126]
Cassava starch

Sunflower oil cake (SOC)

(0 to 20%wt of solids)

Urea as blowing agent Compression thermoforming 3 0.15–0.23 (increases with filler content) 113–139 μm (decreases with filler content)

Flexion test

σma = 1.88–2.61 MPa

Compression test

Hd = 2.39–6.9 kgf

Ene = 18.4–50.8 mJ

12–14.3%

41.9–50.4 g water/gDB

Biocomposite foams expanded with urea show greater biodegradability [126]
Cassava starch Cassava inner bark (0–50%wt of solids) Starch gelatinizing Compression thermoforming 2.9–3.2 0.021–0.032 -

Flexion test

σma = 1.8–4.5 MPa

εBb = 0.80–1.30%

(filler decrease flexibility)

2.78–5.29 g water/gDB Biocomposites with the incorporation of cassava inner bark presented lower water absorption [405]
Cassava starch + Chitosan (0–6%wt) Kraft fiber (0–40%wt of starch) - Compression thermoforming - 0.11–0.15 -

Tensile test

σma = 0.30–1.17 MPa

εBb = 1.68–2.07%

8.07–15.2 g

water/gDB (decreases with fiber content)

Solubility decreased with chitosan and fiber addition [377]
Oca starch Sugarcane bagasse (0 to 40%wt of solids) - Compression thermoforming 2.57–2.60 0.157–0.272 -

Flexion test

σma = 0.5–0.79 MPa

εBb = 0.60–1.10%

64.9–94.7 g water/gDB SB addition above 20% decreases water absorption capacity and mechanical resistance [372]
Oca starch Asparagus peel fiber (0 to 40%wt of solids) - Compression thermoforming 2.49–2.61 0.144–0.291 -

Flexion test

σma = 0.51–0.62 MPa

εBb = 0.90–1.60%

79.2–93.8 g water/gDB Biocomposite density decrease at low filler content [372]
Wheat starch Barley straw, grape and cardoon filler (0 and 5%wt of solids) - Extrusion, thermo-compression and microwave foaming 2.1 292–347 200–600 μm (average with a wide size range)

Compression test

σma = 1.24–2.18 MPa

Ec = 43.7–52.8 MPa

Wf = 1.91–4.54 mJ m−3

1 − 2.5% Barley straw fibers use result in tougher biocomposites foams [383]
Citric acid cross-linked potato starch

Microcrystalline cellulose powder

(25%wt of solids)

Carnauba wax as mold release and hydrophobic agent Compression thermoforming 2.2 - Cross-linked starch biocomposites show higher cell-density structures

Tensile test

σma = 1.76 − 2.25 MPa

εBb = 1.20 − 1.97%

Flexion test

σma = 3.76 − 7.61 MPa

Ec = 445 − 600 MPa

- Foams crosslinked with 5% citric acid presented the better mechanical properties [376]
PLA

Sepiolite

(0 − 10%wt of total solids)

Commercial chemical foaming agent (CFA) Injection molding 4 0.82 − 1.30 (increases with filler content, decrease with CFA) Biocomposite foams show smaller cell size and a higher cell density because nanoclay acts as cell nucleating sites

Flexion test

σma = 36.6 − 121.8 MPa

εBb = 1.79 − 8.89%

Ec = 1883–3464 MPa

- The incorporation of nanoclays down to a 5%wt load improves the toughness of the nanocomposite but greater amounts act in detriment of it [382]
PLA Kenaf fiber powder (20%wt of solids) Azodicarbonamide (ADC) as foaming agent Extrusion and thermopressing 3 0.87–1.13

61–78 μm

(lower extrusion temperature)

Tensile test

σma = 2.77 − 18.66 MPa

2.7 − 3.0%

0.05–0.24 g water/gDB (increases with blowing agent content)

- [79]
Alginate Orange peel (10%wt) + CaCO3 (10%wt) - Oven dried (35 °C for 4 days) 1–3 40–42 Pore-size is difficult to quantify because of shape irregularities but were estimated to range between 100–500 μm Mechanical properties comparable to those of commercial fire-retardant PU 14.67 ± 0.65%

Fire retardant properties and less hazardous combustion gases production than PU

k g = 0.03 W m−1 K−1 Cp f = 1600 J kg−1 K−1

[338]
PBS

Cellulose Nanocrystals (CNC)

(0–0.5%)

CNC acetylation Melt mixing and supercritical CO2 1 0.033–0.144 (decreases with filler)

27.7–33.2 μm

0.72–1.06 109 cells cm−3

- -

Thermal insulation increase with filler k g decrease from 0.063 to 0.21–

0.27 W m−1 K−1

[406]

aMaximum strength (σm); (TD); belongation at break (εB); celastic modulus (E); dhardness (H); ecompression energy absorption (En); fcompression energy absorption per unit volume (W); gthermal conductivity (k); hspecific heat (Cp)