Table 4.
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)