Natural rubber latex (NRL) is a biopolymer consisting of isoprene monomers in a cis configuration connected by double bonds that can degrade naturally. Most natural rubber (NR) based products are single-use items and its microbial degradation process is relatively slow. Hence, this review highlights the importance in the enhancement of biodegradation of NR, the methods applied to increase the biodegradation rate, and characterization of biodegradation of rubber. The biodegradability of NR-based products is enhanced via selective microorganism strains, suitable composting environment and the addition of biofillers. Rubber oxygenase enzymes and latex cleavage protein are major contributors in the biodegradation of NR-based products, while biofillers such as chitosan, cellulose whiskers and starch enhances biodegradation rate up to 60 %. Biodegradation of NR-based products is confirmed through characterization of physicochemical, thermal and mechanical properties using SEM, XRD, FTIR, GPC, TGA, UTM, physical appearance and weight loss. NR-based materials with enhanced biodegradability have many uses, thus its customizability should be studied further in terms of different product forms, fabrication method, orientation of biofiller used and incorporation of metal organic frameworks.

Environmental issues caused by plastic films promote the development of biodegradability packaging materials. Copper ion-modified nanocellulose films were prepared through a one-pot reaction and systematically investigated their structural characteristics, thermal stability, mechanical properties, antibacterial activity, and biodegradability. The results indicate that the film prepared by co-soaking CNCs and copper in NaOH solution for 12 h has favorable performance. Introduction of copper ions as crosslinkers increases tensile strength of film from 36.8 MPa to 56.4 MPa and water contact angle of film from 46 degrees to 92 degrees. Copper coordination also endows the film excellent antibacterial activity, inhibiting growth of Escherichia coli and Staphylococcus aureus. Moreover, biodegradability tests indicate that although the introduction of copper ions slightly reduce biodegradation rate of films, they could still be decomposed significantly within four weeks as burying in soil. This simple process for preparing cellulosic films with water resistance, thermal stable, antibacterial ability, and biodegradable shows potential application in flexible packaging film.

This study explored mycelium-based composites (MBCs) as a sustainable alternative to conventional materials, focusing on the role of lignocellulosic substrates in optimizing their physical, mechanical, and biodegradability properties. It also addressed the valorization of agroforestry by-products, particularly European hazelnut shells (HZ) and radiata pine sawdust (SW), in an effort to reduce waste and minimize environmental impacts. The MBCs were obtained using two formulations (HZ100 and HZ75-SW25) of local agroforestry by-products bound together with natural growth of fungal mycelium from Ganoderma sp. We examined the physical and mechanical properties of these novel materials, including the density, shrinkage, water absorption, hydrophobicity, moduli of rupture and elasticity, and internal bond strength. Additionally, we assessed the biodegradability of the MBCs in soil to estimate the time required for complete degradation. The results clearly indicated differences in performance between the MBCs from HZ100 and HZ75-SW25. In general, HZ75-SW25 demonstrated superior mechanical performance compared to HZ100. Water absorption was low in both cases, suggesting a degree of hydrophobicity on the surface. The biodegradation results indicated that the fabricated MBCs could fully decompose in less than one year when buried in soil, confirming that these biocomposites are entirely biodegradable.

In this study, novel block copolymers consisting of poly(ethylene succinate) (PES) and poly(amino acid)s were synthesized, and their thermal and mechanical properties and biodegradability characteristics were investigated. Various types of poly(amino acid) units were successfully introduced using N-phenyloxycarbonyl amino acids (NPCs). The reactions between the terminally aminated PES and the NPCs were conducted by heating in N,N-dimethylacetamide at 65 degrees C. Structural analyses of the obtained polymers confirmed that the reaction with the NPCs proceeded from both ends of the terminally aminated PES. The results of material property measurements demonstrated that the melting point of the block copolymer containing poly(alanine) units increased beyond 200 degrees C while that of the original PES was similar to 100 degrees C. Additionally, its strain at break increased similar to 80-fold compared to that of PES with a similar molecular weight. The results of biodegradability tests using a soil suspension as an inoculum indicated that some of the block copolymers underwent biodegradation, and a correlation was observed between the biodegradability and the type and feed amount of NPC. Therefore, it was proposed that the degree, rate, and onset time of biodegradation could be controlled by altering the type and amount of incorporated poly(amino acid) units. This research may contribute to the optimal and facile synthesis of polyester-b-poly(amino acid) copolymers and to the expansion of the range of available biodegradable materials.

Preparation and characterization of biopolymer-based packaging materials have significantly gained importance because of sustainability, biodegradability, and eco-friendly nature. In this study, novel wheat gluten (WG)/cloisite 30B (C30B) organoclay-based bionanocomposite (BNC) films were prepared by solution casting method at various C30B concentrations (5%, 10%, and 15%). X-ray diffraction and field emission scanning electron microscopy revealed intercalation/exfoliation of C30B sheets into the WG matrix. WG-C30B 10% film was thermostable. It showed low surface roughness along with higher water barrier properties and surface hydrophobicity. The tensile strength values of WG and WG-C30B 10% films were found to be 0.7 +/- 0.02 and 1.11 +/- 0.01, respectively, indicating improvement in mechanical properties. WG-C30B 10% film demonstrated antibacterial activity against both Staphylococcus aureus and Salmonella enterica. Shelf life of green grapes was monitored under different conditions: 4 degrees C, ambient conditions, and 42 degrees C. WG-C30B 10% film proved effective in extending shelf life up to 18 days under ambient conditions. More than 50% of the bionanocomposite films were degraded in agricultural soil within 2 weeks, while completely degraded in sewage sludge soil after a few days. WG-C30B 10% film appeared to be promising regarding the demonstrated physico-chemical and antibacterial properties. This report would be useful in preparing biodegradable biopolymer-based packaging materials.

The need for renewable and biodegradable materials for packaging applications has grown significantly in recent years. Growing environmental worries over the widespread use of synthetic and non-biodegradable polymeric packaging, particularly polyethylene, are linked to this increase in demand. This study investigated the degradation properties of low-density polyethylene (LDPE), a material commonly used in packaging, after incorporating various natural fillers that are sustainable, compatible, and biodegradable. The LDPE was mixed with 2.5, 5, and 10 wt.% of sawdust, cellulose powder, and Nanocrystalline cellulose (CNC). The composites were melted and mixed using a twin-screw extruder machine with a screw speed of 50 rpm at 190 degrees C to produce sheets using a specific die. These sheets were used to prepare samples for rheological tests that measured the viscosity curve, the flow curve, and a non-Newtonian mathematical model using a capillary rheometer at 170, 190, and 210 degrees C. X-ray diffraction analysis was carried out on the 5 wt.% samples, and a short-term degradation test was conducted in soil with a pH of 6.5, 50% humidity, and a temperature of 27 degrees C. The results revealed that the composite melts exhibited non-Newtonian behavior, with shear thinning being the dominant characteristic in the viscosity curves. The shear viscosity increased as the different cellulose additives increased. The 5% ratio had a higher viscosity for all composite melts, and the LDPE/CNC melts showed higher viscosities at different temperatures. The curve fitting results confirmed that the power-law model best described the flow behavior of all composite melts. The LDPE/sawdust and cellulose powder melts showed higher flow index (n) and lower viscosity consistency (k) values compared with LDPE/CNC melted at different temperatures. The sawdust and powder composites had greater weight loss compared with the LD vbbPE/CNC composites; digital images supported these results after 30 days. The degradation test and weight loss illustrated stronger relations with the viscosity values at low shear rates. The higher the shear viscosity, the lower the degradation and vice versa.

To address the depletion of non-renewable resources and align with the principles of green development, researchers increasingly turned to natural plant extracts to synthesise bio-based waterborne polyurethanes (BWPU) as a sustainable alternative to conventional petroleum-derived BWPUs. Although BWPU demonstrated low emissions and non-toxic characteristics, they still exhibited limitations in heat resistance and relatively reduced biodegradability. Thus, to enhance the overall performance of BWPU, sorbitan monooleate (SP) and quercetin (QC) were incorporated into the formulation of hybrid waterborne polyurethane (CWPU). As natural bio-based hybrid materials, QC and SP facilitated the formation of cross-linking networks and hydrogen bonds, enhancing intermolecular interactions and conformational stability in self-cross-linking CWPU. The research concentrated on investigating the chemical structure, mechanical properties, thermal characteristics, and biodegradability of CWPU. The results demonstrated that the introduction of QC constructed a dense cross-linking network, leading to an increase in elongation at the break of CWPU from 460 % to 864 %. Under the condition of 5 % weight loss (T5%), the thermal stability of CWPU was significantly enhanced, with the decomposition temperature increasing from 200 to 243 degrees C. In addition, after degradation in soil and in a 0.6 % lipase PBS buffer for 28 days, the weight of CWPU decreased to 53 % and 48 %, respectively. CWPU can optimise the utilisation of BWPU in biomedical and packaging applications, thereby contributing to innovations in environmentally friendly materials.

The pervasive use of petroleum-based food packaging has caused significant ecological damage due to their unsustainability and non-biodegradability. Polysaccharide-based biodegradable materials are promising alternatives, but low hydrophobicity and functional properties limit their practical applications which can be overcome by incorporation of phytochemical(s). Therefore, by leveraging the strong antioxidant and antibacterial potential of pterostilbene (PTB), we have developed PTB nanoemulsion (NE) incorporated chitosan/sodium alginate (CS/SA) film for food packaging applications. The PTBNE was prepared by high pressure homogenization and characterized for particle size distribution and morphology via DLS, TEM and AFM. The PTBNE CS/SA film was developed by solvent casting method and demonstrated improved mechanical, optical, water resistance and oxygen barrier properties as compared to native CS/SA film. The films were characterized via SEM, 3D optical profilometry, FTIR, XRD and TGA analysis to assess morphological and structural variations. Notably, incorporation of PTBNE in CS/SA matrix significantly enhanced the antioxidant and antibacterial potential of film along with biocompatibility in fibroblast cells. The developed PTBNE CS/SA film demonstrated comparable results with polythene in post harvested shiitake mushroom preservation up to 10 days with rapid soil degradation. Overall, the findings suggested that PTBNE CS/SA film can be a promising alternative to conventional petroleum-based packaging materials.

A novel thermoset biopolymer was developed from citric acid and glycerol (referred to as Polyglycerol citrate (PGC)) through polycondensation. PGC is a completely biodegradable and water-soluble polymer, but it has poor thermal stability, fire retardant and mechanical properties. To enhance the usability of this material in food packaging, insulations, and other domestic products, its strength was enhanced by reinforcement through jute fiber (JF) which is also biodegradable and environmentally friendly. The thermal stability and fire-retardant properties of the jute/PGC composite were improved by incorporating aluminum trihydride (ATH) particles in it. The concentration of ATH was varied between 0% and 12% to evaluate the optimum composition for improved thermal, mechanical and flammability properties. The strength and modulus of the material were evaluated using a tensile test while the fire retardant and thermal properties were determined using burning tests, cone calorimetry and thermogravimetric analysis. The surface morphology was studied through a scanning electron microscope. The maximum tensile strength was obtained by incorporating 9% ATH in the jute/PGC composite, which is 236% higher than the strength of neat PGC resin. Similarly, the heat release rate of jute/PGC composite was reduced by 17% with the incorporation of ATH particles. Also, the burning rate of jute/PGC was reduced by 72%. Thermal stability was also observed to improve. Possible chemical interaction between the constituents of the composite was confirmed through Fourier transform infrared spectroscopy (FTIR). The biodegradation of the composite specimens was validated through a soil burial test.

Biodegradable plastic is the preferred alternative to traditional plastic products due to its high degradability, decreased dependence on fossil sources, and decreased global pollution according to the accumulation of traditional plastic. In the current study, the optimization of biodegradable plastic synthesis was studied using biomass reinforcement materials. The reinforcement material is cellulose extracted from sawdust to prepare biodegradable plastic using the casting method. Response surface methodology using Box-Behnken Design is used to optimize the main parameters affecting the tensile strength and elongation at the break of the biodegradable plastic. These parameters are cellulose fiber addition, acetic acid addition, and the mass ratio of glycerol to starch. The maximum tensile strength and elongation were obtained at 4.45 MPa and 5.24%, respectively, using 5% cellulose fiber addition and 11.24% acetic acid addition with a 0.266 w/w glycerol to starch mass ratio. Various analyses were performed on the produced biodegradable plastic, including FTIR, SEM, and thermal stability. The biodegradability of the produced biodegradable plastic after immersing the soil for 10 days was about 90% higher than the traditional plastics. The produced biodegradable plastic has a moisture content of 4.41%, water absorption of 81.5%, water solubility of 24.6%, and alcohol solubility of 0%. According to these properties, the produced biodegradable plastic can be used in different industries as a good alternative to traditional plastics.