Biodegradable Polyester Research Articles

Effect of Aging on Tensile and Chemical Properties of Polylactic Acid and Polylactic Acid-Like Polymer Materials for Additive Manufacturing.

Additive manufacturing, with its fast development and application of polymeric materials, led to the wide utilization of polylactic acid (PLA) materials. As a biodegradable and biocompatible aliphatic polyester, produced from renewable sources, PLA is widely used in different sectors, from industry to medicine and science. The aim of this research is to determine the differences between two forms of the PLA material, i.e., fused deposition modeling (FDM) printed filament and digital light processing (DLP) printed resin, followed by aging due to environmental and hygiene maintenance conditions for a period of two months. Specimens underwent 3D scanning, tensile testing, and Fourier transform infrared (FTIR) spectrometry to obtain insights into the material changes that occurred. Two-way Analysis of Variance (ANOVA) statistical analysis was subsequently carried out to determine the statistical significance of the determined changes. Significant impairment can be observed in the dimensional accuracies between both materials, whether they are non-aged or aged. The mechanical properties fluctuated for aged FDM specimens: 15% for ultimate tensile stress, 15% for elongation at yield, and 12% for elastic modulus. Regarding the DLP aged specimens, the UTS decreased by 61%, elongation at yield by around 61%, and elastic modulus by 62%. According to the FTIR spectral analysis, the PLA materials degraded, especially in the case of resin specimens. Aging also showed a significant influence on the elastic modulus, ultimate tensile stress, elongation at yield, elongation at break, and toughness of both materials, which was statistically shown by means of a two-way ANOVA test. The data collected in this research give a better understanding of the underlying aging mechanism of PLA materials.

Comprehensive study of antimicrobial polycaprolactone/clay nanocomposite films: Preparation, characterization, properties and degradation in simulated body fluid

AbstractEven though the biodegradability of polycaprolactone (PCL) and its nanocomposites is lower compared to other biodegradable polyesters, this property and good biocompatibility are used for development of materials for drug delivery with a long‐term effect. We prepared novel PCL/clay nanocomposite films with antimicrobials chlorhexidine (CH) or octenidine (OCT) combined with ZnO anchored on vermiculite (VER). The intercalation of CH and OCT into the interlayer of VER/ZnOVER was confirmed by XRD, FTIR and SEM. The organically modified nanofillers compared to VER (−46.0 mV) or ZnOVER (−34.9 mV) showed a positive ζ‐potential (+30.7 mV (VER_CH), +21.9 mV (VER_OCT), +24.6 mV (ZnOVER_CH)) indicating a relatively stable materials, except ZnOVER_OCT (+8.6 mV), which strongly agglomerated.Thin PCL/clay films were prepared by solvent casting method and the effect of used nanofillers on structural, thermal, mechanical and antimicrobial properties followed by degradation under hydrolytic conditions was studied. The results showed that presence of ZnO significantly decreases thermal and mechanical stability. The nanofillers with the higher hydrophilic character are responsible for the fastest degradation of PCL matrix. Films possessed high antimicrobial efficiency in long time intervals, hence these nanocomposites open new avenues for the possible application of such materials for the drug delivery with a long‐term effect.Highlights Antimicrobial active PCL/clay nanocomposites were prepared. Nanofillers influenced the structure and properties of prepared thin PCL films. ZnO caused lower thermal stability and worse mechanical properties of PCL films. PCL/clay nanocomposite films degraded slowly by a hydrolytic mechanism. High potential as medical materials with long‐lasting antimicrobial efficacy.

Microrespirometric Validation of a Two-stage Process for Polyhydroxyalkanoates Production from Peanut Oil and Propionate with Cupriavidus necator

Introduction Poly(3-hydroxyalkanoates) (PHA) is a biodegradable polyester synthesized by various bacteria, including Cupriavidus necator. The composition of PHA is influenced by the type of microorganism, cultivation conditions, and carbon substrate. The selection of a carbon source is critical for PHA production, significantly impacting process costs. Therefore, the common goal is scalability, with the design and optimization of PHA production relying on experimental determination of constitutive parameters. Methods In this work, a two-stage process for PHA production was conducted in shaking flasks functioning as mini reactors with the bacteria Cupriavidus necator. During the first stage, fructose was used as the sole carbon source. Once fructose was exhausted, a second stage commenced with a new carbon source, either peanut oil or propionate, to enhance PHA production. Ex-situ pulse respirometry approach was employed during the two-stage process to follow the kinetics of substrate consumption. Results The results indicated that the use of peanut oil would be advantageous over propionate, resulting in 12.2% more biomass and 13.9% more PHA. Conclusion Additionally, the growth rate was 88.9% higher with peanut oil. The characterization by pulse respirometry applied in microreactors, i.e., micro respirometry, allowed for the performance of up to 216 biological experiments to determine four important kinetic and stoichiometric parameters, namely maximum oxygen uptake (rO2max), substrate affinity constant (KS), growth yield (YX/S), and substrate oxidation yield (YO2/S). The values of these parameters indicated that peanut oil would be the best carbon source to promote PHA production during the second stage. The implementation of the microrespirometry technique during the screening of carbon sources for PHA production provided reliable information within a short period and with significantly less experimental effort.

V-doped MoO3 nanorods for highly selective oxidation of 5-hydroxymethylfurfural to bio-monomer 2, 5-furandicarboxylic acid

2,5-Furanodicarboxylic acid (FDCA) is a significant chemical derived from biomass and holds the potential to replace traditional petrochemicals in the production of biodegradable polyester materials. In this study, a series of new-type V-doped MoO3 catalysts with different crystalline phases were prepared through the hydrothermal method. The V-doped α-MoO3 with growth along the [010] crystal plane demonstrated the most efficient catalytic activity in the selective oxidation of 5-hydroxymethylfurfural (HMF) to produce FDCA, potentially attributable to the [010] crystal plane's superior affinity for substrate interactions. The catalysts were analyzed using TEM, XPS, XRD, FT-IR, N2 adsorption isotherms and other characterization techniques. The Box-Behnken response surface method was utilized to investigate and successfully determine the optimal reaction conditions. A remarkable HMF conversion of 99.5% and a 97.4% selectivity toward FDCA were achieved at 80 °C after 10 h using tert-butanol as the solvent and tert-butyl hydroperoxide as the oxidant. Furthermore, the catalyst could be readily recovered conveniently and reused without any significant loss in catalytic activity.

Preparation and Mechanical Properties of PBAT/Silanized Cellulose Composites

Polybutylene adipate-terephthalate (PBAT) is a fully biodegradable polyester, which has been proven to be the most suitable alternative to traditional plastics. However, due to the low strength of PBAT (17.2 MPa) and high price, the use of PBAT has a degree of limitations. To obtain a cost-effective and high-performance composite material of PBAT, for this study we selected microcrystalline cellulose, which is inexpensive and easily available, as the reinforcing medium. However, due to the hydrophobicity of PBAT, the mechanical properties of PBAT when mixed with hydrophilic cellulose were low. In order to improve the compatibility of cellulose and PBAT, this study selected hexadecyltrimethoxysilane (HDTMS) containing long carbon chains to silanize microcrystalline cellulose (MCC) to obtain silanized cellulose (SG). Three types of SGs with different degrees of silanization were obtained by controlling HDTMS with different mass ratios (1:10; 3:10; 5:10) to react with MCC. Characterization of these three types of SGs was conducted using FTIR, TEM, and water absorption analysis. The results demonstrated the successful synthesis of SG. With the increase in the reaction ratio of HDTMS and MCC, the size of the nanoparticles increases, and the water absorption decreases significantly. Subsequently, PBAT/SG composites were prepared by blending three kinds of silanized cellulose with PBAT in different proportions by the sol-gel method. To study the thermal stability and compatibility, the mechanical properties of the composites were evaluated, including thermogravimetric testing, scanning analysis, and dynamic thermomechanical testing. The optimal blending ratio and the optimal type of silane cellulose were found. Analysis of the mechanical properties revealed that the tensile strength initially increased and then decreased with increasing blending ratio for all three composites tested. Among them, the PBAT/SG2 composites exhibit superior performance, with a maximum tensile strength reaching 22 MPa at an 85/15 blending ratio, nearly 30% higher than that of pure PBAT alone. The addition of SG significantly improved the strength of the PBAT, and SG2 is more suitable for preparing high-strength composite materials. In addition, after the addition of SG, the yield stress of the composite is improved while maintaining good thermal stability. Both the SEM and DMA results indicated good compatibility of the PBAT/SG composites. This study provides a new idea for the industrial-scale development of degradable polyesters with low cost and good mechanical properties.

Recyclable and (Bio)degradable Polyesters in a Circular Plastics Economy.

Polyesters carrying polar main-chain ester linkages exhibit distinct material properties for diverse applications and thus play an important role in today's plastics economy. It is anticipated that they will play an even greater role in tomorrow's circular plastics economy that focuses on sustainability, thanks to the abundant availability of their biosourced building blocks and the presence of the main-chain ester bonds that can be chemically or biologically cleaved on demand by multiple methods and thus bring about more desired end-of-life plastic waste management options. Because of this potential and promise, there have been intense research activities directed at addressing recycling, upcycling or biodegradation of existing legacy polyesters, designing their biorenewable alternatives, and redesigning future polyesters with intrinsic chemical recyclability and tailored performance that can rival today's commodity plastics that are either petroleum based and/or hard to recycle. This review captures these exciting recent developments and outlines future challenges and opportunities. Case studies on the legacy polyesters, poly(lactic acid), poly(3-hydroxyalkanoate)s, poly(ethylene terephthalate), poly(butylene succinate), and poly(butylene-adipate terephthalate), are presented, and emerging chemically recyclable polyesters are comprehensively reviewed.

Metabolic engineering of Escherichia coli for high-level production of the biodegradable polyester monomer 2-pyrone-4,6-dicarboxylic acid

2-Pyrone-4,6-dicarboxylic acid (PDC), a chemically stable pseudo-aromatic dicarboxylic acid, is a promising building block compound for manufacturing biodegradable polyesters. This study aimed to construct high-performance cell factories enabling the efficient production of PDC from glucose. Firstly, the effective enzymes of the PDC biosynthetic pathway were overexpressed on the chromosome of the 3-dehydroshikimate overproducing strain. Consequently, the one-step biosynthesis of PDC from glucose was achieved. Further, the PDC production was enhanced by multi-copy integration of the key gene PsligC encoding 4-carboxy-2-hydroxymuconate-6-semialdehyde dehydrogenase and co-expression of Vitreoscilla hemoglobin. Subsequently, the PDC production was substantially improved by redistributing the metabolic flux for cell growth and PDC biosynthesis based on dynamically downregulating the expression of pyruvate kinase. The resultant strain PDC50 produced 129.37 g/L PDC from glucose within 78 h under fed-batch fermentation conditions, with a yield of 0.528 mol/mol and an average productivity of 1.65 g/L/h. The findings of this study lay the foundation for the potential industrial production of PDC.

Production of Polyhydroxyalkanoates for Biodegradable Food Packaging Applications Using Haloferax mediterranei and Agrifood Wastes.

Polyhydroxyalkanoates (PHAs) are high-value biodegradable polyesters with thermoplastic properties used in the manufacturing of different products such as packaging films. PHAs have gained much attention from researchers and industry because of their biobased nature and appropriate features, similar to conventional synthetic plastics. This review aims to discuss some of the recent solutions to challenges associated with PHA production. The implementation of a cost-effective process is presented by following different strategies, such as the use of inexpensive carbon sources, the selection of high-producing microorganisms, and the functionalization of the final materials to make them suitable for food packaging applications, among others. Research efforts are needed to improve the economic viability of PHA production at a large scale. Haloferax mediterranei is a promising producer of PHAs due to its ability to grow in non-sterile conditions and the possibility of using seawater to prepare the growth medium. Additionally, downstream processing for PHA extraction can be simplified by treating the H. mediterranei cells with pure water. Further research should focus on the optimization of the recycling conditions for the effluents and on the economic viability of the side streams reutilization and desalinization as an integrated part of PHA biotechnological production.

Peptide Acylation in Aliphatic Polyesters: a Review of Mechanisms and Inhibition Strategies.

Biodegradable polyesters are widely employed in the development of controlled release systems for peptide drugs. However, one of the challenges in developing a polyester-based delivery system for peptides is the acylation reaction between peptides and polymers. Peptide acylation is an important factor that affects formulation stability and can occur during storage, in vitro release, and after drug administration. This review focuses on the mechanisms and parameters that influence the rate of peptide acylation within polyesters. Furthermore, it discusses reported strategies to minimize the acylation reaction.

Glycerol- and diglycerol-based polyesters: Evaluation of backbone alterations upon nano-formulation performance

Despite the success of polyethylene glycol-based (PEGylated) polyesters in the drug delivery and biomedical fields, concerns have arisen regarding PEG's immunogenicity and limited biodegradability. In addition, inherent limitations, including limited chemical handles as well as highly hydrophobic nature, can restrict their effectiveness in physiological conditions of the polyester counterpart. To address these matters, an increasing amount of research has been focused towards identifying alternatives to PEG. One promising strategy involves the use of bio-derived polyols, such as glycerol. In particular, glycerol is a hydrophilic, non-toxic, untapped waste resource and as other polyols, can be incorporated into polyesters via enzymatic catalysis routes.In the present study, a systematic screening is conducted focusing on the incorporation of 1,6-hexanediol (Hex) (hydrophobic diol) into both poly(glycerol adipate) (PGA) and poly(diglycerol adipate) (PDGA) at different (di)glycerol:hex ratios (30:70; 50:50 and 70:30 mol/mol) and its effect on purification upon NPs formation. By varying the amphiphilicity of the backbone, we demonstrated that minor adjustments influence the NPs formation, NPs stability, drug encapsulation, and degradation of these polymers, despite the high chemical similarity. Moreover, the best performing materials have shown good biocompatibility in both in vitro and in vivo (whole organism) tests. As preliminary result, the sample containing diglycerol and Hex in a 70:30 ratio, named as PDGA-Hex 30%, has shown to be the most promising candidate in this small library analysed. It demonstrated comparable stability to the glycerol-based samples in various media but exhibited superior encapsulation efficiency of a model hydrophobic dye. This in-depth investigation provides new insights into the design and modification of biodegradable (di)glycerol-based polyesters, potentially paving the way for more effective and sustainable PEG-free drug delivery nano-systems in the pharmaceutical and biomedical fields.

Photooxidation‐induced conformational changes and degradation behaviors of poly(butylene succinate) and poly(butylene succinate‐co‐adipate)

AbstractTwo biodegradable polyesters, poly(butylene succinate) (PBS) and poly(butylene succinate‐co‐adipate) (PBSA), were artificially aged in a UV irradiation test chamber, and their photodegradation behaviors investigated. The attenuated total reflection (ATR) infrared (IR) spectra of the initial and UV‐aged samples revealed conformational changes in the tetramethylene sequences of the photoaged PBS and PBSA. The one‐dimensional wide‐angle X‐ray scattering (WAXS) profiles showed that the (110) d‐spacing of the α‐form crystal progressively decreased during UV aging, suggesting that the crystalline polymer chains became arranged more closely along the fiber axis. Accordingly, we conclude that PBS and PBSA transform from their TGTGT to nearly TTTTT conformations upon photoaging. The observed WAXS, small‐angle X‐ray scattering, and IR spectral data suggest that photodegradation preferentially occurs in the amorphous phase of each polymer. The less crystallizable butylene adipate co‐unit enhances the degradability of PBSA, with prolonged photooxidation leading to partial degradation of the crystalline region of the copolymer. This finding is consistent with and may be linked to the higher biodegradability of PBSA compared to PBS.

A natural butter glyceride as a plasticizer for improving thermal, mechanical, and biodegradable properties of poly(lactide acid)

Polylactic acid (PLA) is a biobased and biodegradable thermoplastic polyester with great potential to replace petroleum-based plastics. However, its poor toughness and slow biodegradation rate affect broad applications of PLA in many areas. In this study, a glycerol triester existing in natural butter, glycerol tributyrate, was creatively explored and compared with previously investigated triacetin and tributyl citrate, as potential plasticizers of PLA for achieving improved mechanical and biodegradation performances. The compatibilities of these agents with PLA were assessed quantitively via the Hansen solubility parameter (HSP) and measured by using different testing methods. The incorporation of these compounds with varied contents ranging from 1 to 30 % in PLA altered thermal, mechanical, and biodegradation properties consistently, and the relationship and impacts of chemical structures and properties of these agents were systematically investigated. The results demonstrated that glycerol tributyrate is a novel excellent plasticizer for PLA and the addition of this triester not only effectively reduced the glass transition, cold crystallization, and melting temperatures and Young's modulus, but also led to a significant improvement in the enzymatic degradation rate of the plasticized PLA. This study paves a way for the development of sustainable and eco-friendly food grade plasticized PLA products.

Physical aging of a biodegradable alicyclic polymer: poly (pentamethylene trans-1,4-cyclohexanedicarboxylate)

Physical aging of poly (pentamethylene trans-1,4-cyclohexanedicarboxylate) (PPeCE), a biodegradable alicyclic polyester, was investigated using Fast Scanning Calorimetry (FSC), a recent calorimetric technique allowing to accelerate physical aging and study the associated relaxation processes at different aging temperatures in an experimentally-reasonable time scale. Different mechanisms were highlighted by varying the aging temperature on a temperature range of more than 60 °C. At aging temperatures well below the glass transition temperature, several relaxation mechanisms were evidenced, probably related to secondary relaxation processes (β relaxations). When the aging temperature approaches the glass transition temperature, the primary relaxation process (α relaxation) becomes predominant.

Sustainable Synthesis of Biopolymer Polyhydroxybutyrate (PHB) from Agro-residue by Brevibacterium casei with Emphasis on Degradation Analysis

The Polyhydroxybutyrate (PHB) polymer is a biodegradable microbial polyester that is intracellularly accruing due to the depletion of nitrogen and phosphorous resources and an increase in carbon supply. As part of this research investigation, Sudan Black B staining, fermentation, chloroform-sodium hypochlorite solvent-based extraction, and characterization of extracted PHB were used to isolate and identify organisms capable of producing PHB. Brevibacterium casei (OQ519751) was used to synthesize PHB biopolymer from agro-residues (orange peel, mangosteen peel, sugarcane bagasse, water hyacinth, and jackfruit peel). Using the Response Surface Methodology (RSM) and the Central Composite Design (CCD) has proven to be highly effective for optimizing PHB synthesis. The optimal conditions determined through RSM allowed Brevibacterium casei to produce significant amounts of PHB when compared to an unoptimized medium. The model demonstrated statistical significance, as indicated by the F-value of 19.96 with an associated p-value of <0.0001. Furthermore, with an optimized pH level of 7, temperature of 37°C, and yeast extract as the nitrogen source, the carbon source water hyacinth was found to synthesize an enhanced quantity of a PHB yield of 1.29 g/L from 2.2 g/L of dry biomass (58.63%). PHB characterization was done with the aid of FTIR (Fourier-transform infrared spectroscopy), XRD (X-ray diffraction), and TGA (Thermogravimetric analysis) analysis. The degradation study of PHB films was performed by soil burial method and morphological changes were scrutinized by SEM analysis. The results reveal that utilizing water hyacinth as a feedstock employs an enhanced production of PHB. This is the first report to synthesize maximum yield of PHB from Brevibacterium casei using water hyacinth as a substrate for production.

Experimentally Determined Hansen Solubility Parameters of Biobased and Biodegradable Polyesters.

Hansen solubility parameters (HSP) of 15 commercially relevant biobased and biodegradable polyesters were experimentally determined by applying a novel approach to the classic solubility study method. In this approach, the extent of swelling in polymer films was determined using a simple equation based on the mass difference between swollen and nonswollen film samples to obtain normalized solvent uptake (N). Using N and HSPiP software, highly accurate HSP values were obtained for all 15 polyesters. Qualitative evaluation of the HSP values was conducted by predicting the miscibility of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHB-co-HHx, 7 mol % HHx) and poly(lactic acid) (PLA) with a novel lignin-based plasticizer (ethyl 3-(4-ethoxy-3-methoxyphenyl)propanoate, EP) with a relative energy difference (RED) less than 0.4. Additionally, an HSP-predicted plasticizer (di(2-ethylhexyl) adipate, DA) with a larger RED (>0.7) was used to demonstrate the effects of less-miscible additives. Plasticized samples were analyzed by differential scanning calorimetry and polarized optical microscopy (POM) to determine the Tg depression, with EP showing linear Tg depression up to 50% plasticizer loading, whereas DA shows minimal Tg depression past 10% loading. Further analysis by POM reveals that the DA phase separates from both polymers at loadings as low as 2.5% (PHB-co-HHx, 7 mol % HHx) and 5% (PLA), while the EP phase separates at a much higher loading of 50% (PHB-co-HHx, 7 mol% HHx) and 30% (PLA).

Injection molding of biodegradable polyester blends filled with mineral and sustainable fillers: Performance evaluation

AbstractThis research focuses on the melt processing of biocomposites from a biodegradable polymer blend mixed with hybrid fillers through injection molding technique. An optimized blend ratio (60/40 wt%) poly(butylene succinate‐co‐butylene adipate) (PBSA) and poly(butylene adipate‐co‐terephthalate) (PBAT) demonstrated promising results after blending with a mixture of walnut shell powder (WSP), corn starch and talc in various proportions for use in rigid packaging. The addition of hybrid fillers (i) 10% WSP with 15% talc and (ii) 5% WSP with 5% starch and 15% talc to the polymer blend (60%PBSA/40%PBAT) improved tensile modulus (160% and 162%, respectively) and flexural modulus (147% and 153%, respectively) because of the dispersion of stiffer talc and WSP. Following the addition of fillers, tensile strength of the composites decreased. However, flexural strength improved significantly after filler introduction because of better stress transfer ability. Rheological analysis of filled composites with starch or WSP (25%) depicted similar characteristics of the polymer blend, indicating lower viscosity than hybrid composites. The abundant hydroxyl groups in starch explained the increased water absorption and decreased contact angle compared with other composites. This research's novelty encompasses utilizing low‐cost biomasses with mineral filler into an under‐researched biodegradable polymer blend suitable for single‐use rigid packaging applications.

Microbial decomposition of biodegradable plastics on the deep-sea floor

Microbes can decompose biodegradable plastics on land, rivers and seashore. However, it is unclear whether deep-sea microbes can degrade biodegradable plastics in the extreme environmental conditions of the seafloor. Here, we report microbial decomposition of representative biodegradable plastics (polyhydroxyalkanoates, biodegradable polyesters, and polysaccharide esters) at diverse deep-sea floor locations ranging in depth from 757 to 5552 m. The degradation of samples was evaluated in terms of weight loss, reduction in material thickness, and surface morphological changes. Poly(l-lactic acid) did not degrade at either shore or deep-sea sites, while other biodegradable polyesters, polyhydroxyalkanoates, and polysaccharide esters were degraded. The rate of degradation slowed with water depth. We analysed the plastic-associated microbial communities by 16S rRNA gene amplicon sequencing and metagenomics. Several dominant microorganisms carried genes potentially encoding plastic-degrading enzymes such as polyhydroxyalkanoate depolymerases and cutinases/polyesterases. Analysis of available metagenomic datasets indicated that these microorganisms are present in other deep-sea locations. Our results confirm that biodegradable plastics can be degraded by the action of microorganisms on the deep-sea floor, although with much less efficiency than in coastal settings.

Relationship between Composition and Environmental Degradation of Poly(isosorbide-co-diol oxalate) (PISOX) Copolyesters.

To reduce the global CO2 footprint of plastics, bio- and CO2-based feedstock are considered the most important design features for plastics. Oxalic acid from CO2 and isosorbide from biomass are interesting rigid building blocks for high Tg polyesters. The biodegradability of a family of novel fully renewable (bio- and CO2-based) poly(isosorbide-co-diol) oxalate (PISOX-diol) copolyesters was studied. We systematically investigated the effects of the composition on biodegradation at ambient temperature in soil for PISOX (co)polyesters. Results show that the lag phase of PISOX (co)polyester biodegradation varies from 0 to 7 weeks. All (co)polyesters undergo over 80% mineralization within 180 days (faster than the cellulose reference) except one composition with the cyclic codiol 1,4-cyclohexanedimethanol (CHDM). Their relatively fast degradability is independent of the type of noncyclic codiol and results from facile nonenzymatic hydrolysis of oxalate ester bonds (especially oxalate isosorbide bonds), which mostly hydrolyzed completely within 180 days. On the other hand, partially replacing oxalate with terephthalate units enhances the polymer's resistance to hydrolysis and its biodegradability in soil. Our study demonstrates the potential for tuning PISOX copolyester structures to design biodegradable plastics with improved thermal, mechanical, and barrier properties.

Enhanced biodegradable polyester film degradation in soil by sequential cooperation of yeast-derived esterase and microbial community.

The degradation of biodegradable plastics poses a significant environmental challenge and requires effective solutions. In this study, an esterase derived from a phyllosphere yeast Pseudozyma antarctica (PaE) enhanced the degradation and mineralization of poly(butylene succinate-co-adipate) (PBSA) film in soil. PaE was found to substitute for esterases from initial degraders and activate sequential esterase production from soil microbes. The PBSA film pretreated with PaE (PBSA-E) rapidly diminished and was mineralized in soil until day 55 with high CO2 production. Soil with PBSA-E maintained higher esterase activities with enhancement of microbial abundance, whereas soil with inactivated PaE-treated PBSA film (PBSA-inact E) showed gradual degradation and time-lagged esterase activity increases. The fungal genera Arthrobotrys and Tetracladium, as possible contributors to PBSA-film degradation, increased in abundance in soil with PBSA-inact E but were less abundant in soil with PBSA-E. The dominance of the fungal genus Fusarium and the bacterial genera Arthrobacter and Azotobacter in soil with PBSA-E further supported PBSA degradation. Our study highlights the potential of PaE in addressing concerns associated with biodegradable plastic persistence in agricultural and environmental contexts.

Composite core‐double sheath fibers based on some biodegradable polyesters obtained by self‐organization during electrospinning

AbstractObtaining core‐sheath fibers by single‐spinneret electrospinning is a recent and straightforward approach to prepare composite fibers. Fibers of more complex architecture consisting of poly(ethylene oxide) (PEO) core, inner poly(l‐lactide) sheath sd and outer beeswax (BW) sheath may also be obtained using this method. In the present study we report its applicability for a large series of (bio)degradable polyesters such as poly(ε‐caprolactone), poly(d,l‐lactide‐co‐glycolide), poly(butylene succinate), poly(3‐hydroxybutyrate), and poly(l‐lactide‐co‐d,l‐lactide). The fibers have a well‐differentiated PEO core, polyester inner sheath and BW outer sheath. The possibility for targeted location of hydrophilic or hydrophobic substances in the core or in the sheaths of the PEO/polyester/BW fibers has been demonstrated using nanosized zinc oxide with unmodified (hydrophilic) or silanized (hydrophobic) surface. PEO/polyester/BW fibrous materials loaded with a model drug (5‐nitro‐8‐hydroxyquinoline) exhibit antimicrobial activity. The obtained results show that single‐spinneret electrospinning is a novel and versatile method to prepare core‐double sheath composite fibers prospective for various applications such as biomedicine, cosmetics, and food packaging.