Abstract:In 2021, global petroleum-based plastic production reached over 400 million metric tons (Mt), and the accumulation of these non-biodegradable plastics in the environment is a worldwide concern. Polyhydroxybutyrate (PHB) offers many advantages over traditional petroleum-based plastics, being biobased, completely biodegradable, and non-toxic. However, its production and use are still challenging due to its low deformation capacity and narrow processing window. In this work, two linear-chain polyester oligomers w… Show more
“…Although still modest, this property outperformed the enhancements reported in many other literature sources concerning plasticized PHBV or PHB 14,17,21,63,64 or stood on par with them. 12,15,19,20,24,65 The mechanical properties at freezer condition showed, as expected, an increase of the elastic modulus and the maximum stress. Interestingly, the elongation at break did not change.…”
Section: Mechanical Performance Of Extrusion Blown Films In Service C...supporting
confidence: 79%
“…Notably, the 4% elongation at break was achieved using ATBC. Although still modest, this property outperformed the enhancements reported in many other literature sources concerning plasticized PHBV or PHB 14,17,21,63,64 or stood on par with them 12,15,19,20,24,65 …”
Poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) is a biodegradable polymer with significant potential for use in food packaging. However, its limited melt strength poses a challenge when employing film‐blowing techniques to produce flexible packaging. To overcome this obstacle, we developed blends consisting of 70 wt% PHBV and 30 wt% poly(butylene‐co‐succinate‐co‐adipate) (PBSA). Organic peroxides such as dicumyl peroxide and 2,5‐dimethyl‐2,5‐di‐(tert‐butylperoxy)hexane, were utilized as reactive compatibilizers to enhance the interfacial adhesion between the polymers. Additionally, acetyl tributyl citrate (ATBC) was employed as a plasticizer to improve processability and ductility. The inclusion of organic peroxides resulted in the formation of long‐branched structures, as confirmed by the van‐Gurp‐Palmen plot. The melt flow index decreased from 30 to 9.8 g/10 min without ATBC and 15.5 g/10 min with ATBC. Successful production of blown PHBV/PBSA films was achieved on a pilot scale (bubble height 180 cm). These films exhibited heat‐sealing capability and increased impact strength (7.7 kJ/m2). Moreover, the films maintained a maximum elongation at break of 4% during a 3‐month storage experiment with frozen food. Food safety was assessed through overall migration experiments, and the non‐plasticized films received approval. In conclusion, the compatibilized PHBV/PBSA blends demonstrate great potential as materials for manufacturing film‐blown flexible packaging.
“…Although still modest, this property outperformed the enhancements reported in many other literature sources concerning plasticized PHBV or PHB 14,17,21,63,64 or stood on par with them. 12,15,19,20,24,65 The mechanical properties at freezer condition showed, as expected, an increase of the elastic modulus and the maximum stress. Interestingly, the elongation at break did not change.…”
Section: Mechanical Performance Of Extrusion Blown Films In Service C...supporting
confidence: 79%
“…Notably, the 4% elongation at break was achieved using ATBC. Although still modest, this property outperformed the enhancements reported in many other literature sources concerning plasticized PHBV or PHB 14,17,21,63,64 or stood on par with them 12,15,19,20,24,65 …”
Poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) is a biodegradable polymer with significant potential for use in food packaging. However, its limited melt strength poses a challenge when employing film‐blowing techniques to produce flexible packaging. To overcome this obstacle, we developed blends consisting of 70 wt% PHBV and 30 wt% poly(butylene‐co‐succinate‐co‐adipate) (PBSA). Organic peroxides such as dicumyl peroxide and 2,5‐dimethyl‐2,5‐di‐(tert‐butylperoxy)hexane, were utilized as reactive compatibilizers to enhance the interfacial adhesion between the polymers. Additionally, acetyl tributyl citrate (ATBC) was employed as a plasticizer to improve processability and ductility. The inclusion of organic peroxides resulted in the formation of long‐branched structures, as confirmed by the van‐Gurp‐Palmen plot. The melt flow index decreased from 30 to 9.8 g/10 min without ATBC and 15.5 g/10 min with ATBC. Successful production of blown PHBV/PBSA films was achieved on a pilot scale (bubble height 180 cm). These films exhibited heat‐sealing capability and increased impact strength (7.7 kJ/m2). Moreover, the films maintained a maximum elongation at break of 4% during a 3‐month storage experiment with frozen food. Food safety was assessed through overall migration experiments, and the non‐plasticized films received approval. In conclusion, the compatibilized PHBV/PBSA blends demonstrate great potential as materials for manufacturing film‐blown flexible packaging.
“…Additionally, it was impossible to distinguish the T g value of the PHB in the DSC curves. However, in the literature this value is in the −10°C and 15°C range, depending on the supply source 43,49 …”
Section: Resultsmentioning
confidence: 99%
“…However, in the literature this value is in the À10 C and 15 C range, depending on the supply source. 43,49 3 and Figure 5, the NR fibrous mat revealed characteristics typical of elastomeric polymers: a high elongation at break (ε at break ) of 738 ± 36% and a tensile strength at break (σ at break ) of 2.01 ± 0.28 MPa. On the other hand, as NR was partially replaced by PHB to form a NR-PHB fibrous bioblend, the specimen revealed a reduction in ε at break and an increase in σ at break compared to the NR fibrous mat, in which values were equal to 477 ± 25% and 4.11 ± 0.08 MPa, respectively.…”
The solution blow spinning technique was used to fabricate a new biocomposite fibrous mat consisting of natural rubber (NR) and polyhydroxybutyrate (PHB) bioblend, with various loads of 45S5 bioglass (BG) particles. According to SEM analysis, NR fibers exhibited ribbon‐like morphologies, whereas the addition of PHB resulted in improved fiber formation and a reduction in their diameter. In NR‐PHB/BG biocomposites with varying BG loadings, typical thermal degradation events of PHB (stage i) and NR (stage ii) were observed. In comparison with pure PHB, the TG/DTG curves of NR‐PHB/BG specimens revealed a lower stage i degradation peak. Such an outcome is possibly due to the fact that PHB in the NR‐PHB fibers is located predominantly at the surface, that is, PHB is more susceptible to thermal degradation. The NR‐PHB/BG biocomposite possessed an increased stiffness due to the addition of PHB and BG, resulting in an increased stress and a decreased strain at rupture compared to the pure NR and NR‐PHB mats. DMA analysis revealed two well‐defined regions, above and below the glass transition temperature (Tg), for the storage modulus (E') of the NR‐PHB/BG specimens. The values of E' were in both regions for NR‐PHB/BG specimens increased at higher BG content. The measured tanδ = E″/E' was used to determine the Tg value for all specimens, with Tg found to be in the −49 to −46°C range. Finally, NR‐PHB/BG biocomposite fibrous were proven noncytotoxic by in‐vitro testing on fibroblasts. These biocomposites enhanced cell growth, holding great promise for tissue engineering applications.Highlights
Solution blow spinning technique was used to produce three‐phase biocomposite specimens.
NR‐PHB/BG fibrous mat specimens with a diameter of 9–10 μm were obtained.
Although high BG loads are applied to the NR‐PHB/BG specimens, they remain elastic and flexible.
Fibrous biocomposite mats enhance cell growth and possess great potential for tissue engineering.
“…Poly(3-hydroxybutyrate) (PHB) and its copolymers show good biodegradability even in marine environments [1][2][3], which makes them attractive to replace conventional plastics; e.g., isotactic polypropylene (PP). To date, various basic properties of PHB and its copolymers have been clari ed, such as rheological properties in the molten state [4][5][6], thermal properties including crystallization behavior [1,2,[7][8][9][10], processability [2,11,12], mechanical properties in the solid state [1,2,[13][14][15][16][17], structure and properties of blends and composites with other materials [15,[18][19][20][21][22][23], and degradation behavior [1-3, 24, 25]. The melting point (T m ) of PHB is approximately 180°C and decreases with increasing comonomer content [1,2].…”
The mechanical responses during loading, unloading, and reloading cyclic tensile tests of a tubular blown film of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) are studied. Although the stress–strain curve recorded during the initial stretching process is typical for a crystalline polymer, the stretched film behaves like a rubber during the reloading process; that is, low modulus with a small residual strain after unloading. Furthermore, the stress–strain curves during the reloading process are an inverted “S” shape. During the first stretching process of the polymer film, small crystals are destroyed without reorganization into a crystalline structure, leading to the observed decrease of crystallinity. In contrast, well-developed crystals that orient to the machine direction of the film do not disappear during the first stretching and act as crosslink points during reloading. As a result, a rubber-like response is detected. This mechanical response during reloading is considerably different from those of conventional crystalline plastics such as polyethylene and polypropylene.
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