Poly Butylene Succinate Research Articles

Effect of Fiber Cross-Sectional and Surface Properties on the Degradation of Biobased Polymers.

Biobased polymers such as polylactic acid (PLA) and polybutylene succinate (PBS) break down naturally under certain environmental conditions. The efficiency of degradation can be linked directly to fiber surface properties, which influence polymer accessibility. Here, the degradation of PLA and PBS fibers with six different cross-sections was investigated. The fibers were aged by hydrolysis and UV exposure in an accelerated weathering test, followed by an ISO 20200 laboratory-scale disintegration test with non-aged fibers as controls. The polymers were analyzed by differential scanning calorimetry, Fourier transform infrared spectroscopy, and gel permeation chromatography, comparing the polymer granulate, virgin fibers, and UV-exposed fibers. It was found that the molecular mass and crystallinity of PBS changed more than PLA during spinning. Several PLA samples were completely degraded, whereas all the PBS samples remained intact. Furthermore, surface openings appeared on the PLA fibers during weathering, suggesting greater sensitivity to UV exposure and hydrolysis than PBS. A clear correlation between the fiber surface area and the degradation rate was observed for all samples, but the correlation was positive for PLA and negative for PBS. The slower degradation of PBS fibers with a larger surface area may reflect the ability of PBS to preserve itself by further crystallization during degradation processes at temperatures higher than the glass transition point. The data clearly show that the analysis of single degradation mechanisms is insufficient to predict the behavior of material under real-world conditions, where different degradation mechanisms may work in parallel or consecutively, and may show interdependencies.

A “core-shell” structure imparting both gas barrier and UV shielding properties for a PLA/ PGA/ PBS ternary blend film

The core-shell structure enhances polymer blend systems by orderly assembly and leveraging complementary properties. This study aims to enhance the flexibility and barrier properties of polylactic acid (PLA, L) by blending it with polyglycolic acid (PGA, G) for gas barrier and polybutylene succinate (PBS, B) for flexibility. Encapsulating PGA in a core-shell structure using PBS resolves PGA's rapid hydrolysis issue. The theoretical models predicting dispersion patterns based on spreading coefficients and interfacial tensions were validated through SEM observations, confirming the formation of a core-shell structure in the 5L1G4B ternary blend. Compared to the PLA/PBS binary blend film, samples with PGA (5L1G4B and 4L1G5B) exhibit higher elongation at break and tearing strength. For instance, the elongation at break of the 5L1G4B sample increases from 272.3 % of 6L4B to 470.85 %. The 5L1G4B showed comparable oxygen and carbon dioxide barrier properties to the 6L4B sample. The 5L1G4B and 4L1G5B samples show <2 % UV transmittance in the UVA region, indicating excellent UV shielding. The 5L1G4B blend film, with its mechanical properties, oxygen barrier, UV resistance, and biodegradability, is ideal for outer layer packaging film and has the potential to replace LDPE in packaging juice and dairy product bottles.

Aluminate-activated nano-SiO2 for enhancing water vapor barrier properties in polymers films: A safe and effective strategy

In this work, a series of nanocomposite films composed of polylactic acid (PLA), poly (butylene adipate-co-terephthalate) (PBAT), polybutylene succinate (PBS), nano-SiO2 activated by aluminate for different times were developed to enhance water vapor barrier properties. The physiochemical and thermal properties of the films were characterized. In addition, total and aluminum migration from the films was monitored, and non-targeted screening was performed to evaluate the potential safety of the composite films. Fourier Transform infrared spectroscopy analysis indicated that the nano-SiO2 was successfully activated by aluminate. Differential scanning calorimetry analysis indicated that incorporation of the activated nano-SiO2 slightly reduced the glass transition temperature (from 54 to 51 °C) and increased the crystallinity degree (from 6.9 % to 11.1 %) of PLA. Incorporation of 0.4 % nanofillers was found to give the highest crystallinity. Thermogravimetric analysis showed that the thermal stability of the PLA/PBAT/PBS films did not change significantly after adding the activated-nano-SiO2. However, the incorporation of these nanofillers did increase the interfacial roughness and crystallinity degree of the films, thereby reducing the water vapor permeability by around 30 %. Erucamide was detected in the composite films after exposure to food simulants, however, the films containing the nanofillers still met European Union safety standards. In summary, the nanofiller-loaded polymer films developed in this study were shown to be safe and have high water barrier properties, which means they may be suitable for application in the food, cosmetic, personal care, pharmaceutical, and agrochemical industries.

Investigation of the Influence of Different Filler Contents of Wine Pomace in PBS on Fracture Mechanics Properties

Biobased polybutylene succinate (PBS) represents a promising alternative to petrochemical-based polymers. The use of this biopolymeris limited in many areas by its low resilience against environmental influences. With the help of bio-based stabilizers the thermo-oxidative degradation process can be slowed down. Suitable stabilizing additives are natural antioxidants present in plant extracts with a high flavonoid content, which can be found in grapes, wine and wine by-products. PBS was modified with two different bio-stabilizers based on wine grape pomace. The highest filler content tested was 20 wt.-%. In addition to improving stability, the additives also impact the polymer’s mechanics. The influence of these functional fillers on the fracture mechanical properties was examined in a quasi-static test. The crack growth was recorded using integrated video monitoring. Based on the results, the corresponding crack resistance curve and tearing modulus were determined depending on filler type and content. Additional optical analysis was used to correlate fracture mechanics and structure. The two bio-stabilizers based on red (RWP) and white wine pomace (WWP) differs distinctly in terms of their influence on fracture mechanical properties. The Influence of RWPon the fracture toughness is significantly higher than that of WWP. Especially at lower filler contents with RWP, there is a strong increase in the fracture mechanics parameter tearing modulus (TJ) and an increase in the slope of the R-curve. With 5 wt.% RWP DOM the TJ is 13.64 x 102, whereas with WWP Silv a value of only 6.39 x 102 can be achieved. This difference is also reflected in the increase in the R-curves. With 5 wt.% a slope of the fitted R-curve of 265.59 (RWP DOM) and 121.02 (WWP Silv) could be determined with the first derivative. In the optical analysis it was noticeable that the RWP particles were more homogeneously dispersed in the matrix while the WWP filler tended to agglomerate. The inhomogeneous distribution and strong agglomeration tendency can be attributed to a higher sugar content of WWP and a higher particle size distribution. The top cut (D97) of WWP Silv is 62.37 ± 0.05 µm and that of RWP DOM is 51.97 ± 0.09 µm.

Understanding the Catalytic Efficiency of Two Polyester Degrading Enzymes: An Experimental and Theoretical Investigation.

The discovery of novel plastic degrading enzymes commonly relies on comparing features of the primary sequence to those of known plastic degrading enzymes. However, this approach cannot always guarantee success. This is exemplified by the different degradation rates of the two polymers poly(ethylene terephthalate) (PET) and polybutylene succinate (PBS) by two hydrolases: IsPETase from Ideonella sakaiensis and AdCut from Acidovorax delafieldii. Despite the enzymes showing a very high sequence identity of 82%, IsPETase shows significant hydrolysis activity for both polymers, whereas AdCut only shows significant hydrolysis activity for PBS. By solving the structure of AdCut using X-ray crystallography, and using this as the basis for computer simulations, comparisons are made between the differences in the calculated binding geometries and the catalytic results obtained from biochemical experiments. The results reveal that the low activity of AdCut toward PET can be explained by the low sampling of the productive conformation observed in the simulations. While the active site serine in IsPETase can closely encounter the PET carbonyl carbon, in AdCut it cannot: a feature that can be attributed to the shape of the catalytic binding pocket. These results yield an important insight into the design requirements for novel plastic degrading enzymes, as well as showing that computational methods can be used as a valuable tool in understanding the molecular basis for different hydrolysis activities in homologous polyesterase enzymes.

Mathematical Modelling of Tensile Mechanical Behavior of a Bio-Composite Based on Polybutylene-Succinate and Brewer Spent Grains.

A model based on the fitting of stress-strain data by tensile tests of bio-composites made of a bioplastic (polybutylene succinate (PBS)) and brewer spent grain filler (BSGF) is developed. Experimental tests were performed for various concentrations of BSGF in the range from 2% to 30%. The model is suitable for describing the elastic-plastic behavior of these materials in terms of two mechanical parameters, tensile stress and tensile stiffness (or Young's modulus), depending on the filler concentration. The mechanical characteristics, derived from the fit parameters, show good agreement with the experimental data. The mathematical model used here could be an important aid for the experimentation and manufacturing process as it allows the prediction of the mechanical tensile parameters of a mixture with different filler concentrations, avoiding the long and complex preparation cycle of bio-composites, as well as the specific mechanical tests. The physical properties required by the objects created with the PBS-BSGF bio-composite by the partners/stakeholders of the research project co-financing this research can be quite different; therefore, a mathematical model that predicts some of the mechanical properties in terms of the mixture composition may be useful to speed up the selection of the required amount of BSGF in the mixture.

Effects of Grapevine Fiber and Additives on the Properties of Polylactic Acid Green Bio-Composites

In recent years, numerous researchers have incorporated plant fibers into polymers to alter the thermal and mechanical properties of materials. Grapevines, considered agricultural waste, have led to burdens for farmers and environmental challenges due to their mass production. This study aims to reduce the brittleness of polylactic acid (PLA) by adding polybutylene succinate (PBS) as a toughening agent and employing grapevine fiber (GVF) as a biomass filler. Additionally, the influence of GVF, toughening agents, compatibilizers, and lubrication agents on the tensile strength, heat deflection temperature (HDT), and impact strength of the composites was examined. The findings revealed that the addition of 10% GVF and 5% PBS increased the impact and tensile strengths of PLA from 17.47 J/m and 49.74 MPa to 29.7 J/m and 54.46 MPa, respectively. Moreover, the HDT of the composites exceeded 120 °C when the GVF content was more than 40 wt%. Additionally, the inclusion of a compatibilizer and a lubrication agent enabled the composite containing 30% GVF to achieve tensile and impact strengths of 45.30 MPa and 25.52 J/m, respectively. Consequently, these GVF/PLA green bio-composites not only improve the mechanical and thermal properties of PLA but also promote the reuse of waste grapevines.

Boosting electrochemical performance by regulating rigid-flexible microphase separation of multiblock copolymers

The growth of lithium dendrites and associated safety issues hinder the further development of liquid lithium metal batteries. A novel rigid-flexible multiblock copolymer PBC-mb-PBS was successfully synthesized based on molecular design. Incorporating crystalline rigid phase polybutylene succinate (PBS) into PBC-mb-PBS significantly enhances its tensile strength and low-temperature toughness through physical crosslinking. The flexible polydibutyl 2-(2-cyanoethyl)malonate (PBC) phase with side-chain cyano groups facilitate ionic conduction, forming a LiN-rich stabilized interfacial layer, thereby improving oxidative stability and high-voltage cathode compatibility. A series of multiblock copolymers with varying segment lengths were synthesized to balance mechanical properties and ionic conductivity by adjusting microphase separation. The quasi-solid-state polymer electrolyte (QSPE), derived from PBC-mb-PBS with the molar block ratio of 0.42, exhibits optimal electrochemical performance with ionic conductivity of 6.20 × 10−5 S cm−1 at 30 °C and 4.22 × 10−4 S cm−1 at 60 °C. Due to its bicontinuous microphase structure, it also shows excellent mechanical strength and promotes uniform lithium deposition at high current densities. Li//LiFePO4 and Li//LiNi0.83Co0.05Mn0.12O2 cells demonstrate high capacity retention, confirming the potential of this polymer electrolyte in high-voltage applications. This design strategy offers insights for developing quasi-solid-state lithium metal batteries with superior overall performance.

Application of flow airlift fluidized bed (CAFB) - Aerobic denitrification bioreactor using polycaprolactone (PADR) as organic carbon source and biofilm carrier for synthetic marine aquaculture wastewater treatment

Aerobic denitrification, a novel method for complete nitrate removal process, relies on a constant carbon supply, and carbon availability can be a limiting factor for the process. Three biodegradable polymers - polybutylene succinate (PBS), polycaprolactone (PCL), and polylactic acid (PLA) were used as carbon source of aerobic denitrifying bacteria, Halomonas venusta for treating recirculating aquaculture wastewater in batch tests, respectively. The group utilizing PCL displayed the greatest efficiency in nitrate removal. Afterwards, a continuous flow airlift fluidized bed (CAFB) - aerobic denitrification bioreactor using PCL(PADR) as bio-carriers and carbon source was started up. The effect of shifting temperature on the nitrate removal and microbial community of CAFB-PADR was investigated under different hydraulic retention times (HRT). The results showed that no significant difference was detected in denitrification activity at 25 and 30 °C condition, where the denitrification rate was 1.1–1.8 times higher than that at 15 °C. However, the nitrogen removal efficiency was above 50 % and there was barely accumulation of nitrite at 15 °C, indicating the good nitrate removal performance in CAFB-PADR at all three temperature conditions. Microbial composition analyses revealed that as the temperature decreased, the relative abundance of Gammaproteobacteria increased, while those of Alphaproteobacteria and Bacteroidia diminished decreased. The existence of denitrifying function genera (Marinobacter, Pseudomonas, Halomonas and Hydrogenophaga) ensured the rapid removal of nitrogen in the biofilter. When the temperature dropped to 15 °C, Pseudomonas progressively took the position of Marinobacter, both of which had denitrification and degradation activities. The relative abundance of the denitrifying bacteria Halomonas that we inoculated has been less than 1 % since phase II. Overall, the PCL-supported CAFB-PADR demonstrated in this study shows potential for removing high concentrations of nitrate from recirculating marine aquaculture wastewater.

The effect of biodegradable polymer blending on the disintegration rate of PHBV, PBS and PLA in soil

This study generates new insights into the disintegration phenomena that take place upon blending different classes of biodegradable polymers. Polymer blending is found to be an effective method to tailor the disintegration rate of these polymers in soil. It is shown that the biodegradation of poly(hydroxybutyrate-valerate) (PHBV) can be accelerated by blending with polybutylene succinate adipate (PBSA) and polycaprolactone (PCL). The observed high rate of disintegration of polybutylene succinate (PBS) in soil (severe deterioration in 4 weeks, and fragmentation in 4 months) does not fully align with its current reputation in the market as a polymer that is non-biodegradable in soil. Disintegration trials executed in soil media with different inoculants demonstrate that the biodegradation rate of PBS in soil is highly dependent on the specific soil conditions. Moreover, it is shown that the biodegradation of PBS can be substantially accelerated by blending it with PBSA (fragmentation in 8 weeks). Finally, it is shown that the disintegration of polylactic acid (PLA) in soil can be enhanced by blending it with PCL. Experiments that monitor the CO2 evolution of these blends, both in soil and in home composting environments, demonstrate that not just the disintegration, but also the overall biodegradation of PLA is enhanced by blending with PCL (39% conversion to CO2 in 12 months incubation in soil; 89% conversion to CO2 in 6 months incubation in home composting conditions). This opens up possibilities for targeted blending strategies to reduce potential accumulation of PLA-based plastics in soil environments.

Absence of synergistic effects between microplastics and copper ions on the spread of antibiotic resistance genes within aquatic bacteria at the community level

Microplastics and copper ions (Cu2+) are favorable in accelerating the propagation of antibiotic resistance genes (ARGs) in the plastisphere, however, their combined effects on the ARG spread within the bacterial community of the natural environment were less understood. The influence of microplastic types and Cu2+ concentrations on the horizontal gene transfer (HGT) of ARGs mediated by RP4 plasmid within natural bacterial communities in aquatic environments was investigated. Both biodegradable polybutylene succinate (PBS) and non-biodegradable polyvinyl chloride (PVC) microplastics significantly enhanced the transfer of ARGs, with PBS showing a significant higher effect compared to PVC. Cu2+ also increased transconjugation rates at environmentally relevant concentrations (5 μg L−1), but higher levels (50 μg L−1) lead to decreased rates due to severe bacterial cell membrane damage. The transconjugation rates in the presence of both microplastics and Cu2+ were lower than the sum of their individual effects, indicating no synergistic effects between them on transconjugation. Proteobacteria dominated the composition of transconjugates for all the treatment. Transmission electron microscope images and reactive oxygen species production in bacterial cells indicated that the increased contact frequency due to extracellular polymeric substances, combined with enhanced membrane permeability induced by microplastics and Cu2+, accounted for the increasing transconjugation rates. The study provides valuable insight into the potential effects of microplastics and heavy metals on the spread of ARGs from donors to bacterial communities in natural environments.

Eco-friendly, high-hydrophobic polybutylene succinate foam for oil-water separation

Polybutylene succinate (PBS) is an excellent biodegradable resin with good processability and toughness. The inherent hydrophobicity of this material makes it unique for the preparation of oil-water separation materials. In this paper, PBS foams with high hydrophobicity were prepared by the non-solvent induced phase separation (TINIPS) method using N, N-dimethylformamide (DMF) as a good solvent and anhydrous ethanol as a non-solvent. The effect of PBS concentration on the wettability and micro-morphology of this foam was experimentally investigated. The results showed that the foam had an optimal microporous structure with a water contact angle as high as 145° when the concentration of PBS was 30 %. It was further found that the saturated adsorption capacity of the foam was 5.55–12.39 times its mass and remained strong after 10 adsorption tests. Finally, the environmental adaptability of foams had been studied. The foams maintained their superhydrophobic and oil-absorbing properties in the presence of strong acids, strong bases, saturated sodium chloride solutions, and repeated abrasion. In addition, with the help of a pump-assisted adsorption device, oil-water mixtures can be separated continuously and quickly. This showed that the material had a broad application prospect in oil-water separation.

Enhancing nitrogen removal by simultaneous nitritation and denitritation in a multi-cycle SBR with supplementation of solid carbon sources

Simultaneous nitritation and denitritation have the potential to significantly improve nitrogen removal in sewage treatment processes. However, their application in low-strength sewage treatment systems presents challenges. This study explored the impact of four solid carbon sources (SCSs) on N-removal via nitrite in a multi-cycle SBR with biocarriers. Results showed that both N-removal efficiencies and nitrite accumulation rates increased with higher COD/N ratios, indicating that high COD/N ratios can improve the competition between denitrifiers and nitrite-oxidizing bacteria for nitrite, leading to stable simultaneous nitritation and denitritation. The supplementation of SCSs further enhanced this high-efficiency N-removal process, with polybutylene succinate (PBS) and polycaprolactone (PCL) showing greater increases in N-removal via nitrite than poly-hydroxybutyrate (PHB) and poly-hydroxyalkanoate (PHA). Moreover, PBS showed the most significant increase in denitrification efficiency in anoxic conditions, while PHA was the most effective external SCS at a moderate level of dissolved oxygen. These findings suggest that the incorporation of external SCSs can facilitate the simultaneous nitritation and denitrification process in multi-cycle SBRs, underscoring the importance of selecting an appropriate SCS for optimizing nitrogen removal in sewage treatment projects.

Investigating the effect of GO‐ZnO nano‐hybrid on the mechanical, rheological, and degradation performance of poly (butylene succinate)

AbstractThis paper reports on preparing two types of graphene oxide‐zinc oxide (GO‐ZnO) nano‐hybrids and their effect on the performance of polybutylene succinate (PBS) matrix. This view synthesized GO, ZnO, and GO‐ZnO nano‐hybrids at 1:1 and 1:2 weight ratios. Subsequently, various spectroscopy and microscopy analyses (FTIR, UV, Raman, AFM, and TEM) were employed to characterize the structure of synthesized nanomaterials. The obtained results revealed that the hybridization was successfully occurred and microstructure of two types of prepared nano‐hybrids are basically different depending on the preparation procedure. Following this, PBS nanocomposites with 0.5, 1, and 1.5 wt% of GO‐ZnO nano‐hybrids (NPs) were produced via the solvent‐blending method. The mechanical, microstructural, rheological, biodegradability and UV‐shielding properties of the fabricated films were then investigated. Mechanical properties showed that addition of 0.5 wt% ZnO‐GO nanohybrids improved elongation at break from 21.6% to 28.7% and increased tensile strength by 20%. However, rheological assessments showed a one‐order‐of‐magnitude decrease in viscosity with the addition of only 0.5 wt%. In degradation analysis, 100 percent of mass loss was observed during 5 weeks for PBS with 1.5 wt% of GO‐ZnO. PBS/GO‐ZnO nanocomposites indicated tailored mechanical properties, biodegradability, suggesting a promising potential in packaging applications.Highlights GO‐ZnO nanohybrids were successfully synthesized. Incorporating GO‐ZnO into PBS improved its hydrolytic degradation The thermal decomposition of PBS was accelerated by the addition of GO‐ZnO. Adding GO‐ZnO nanohybrids to PBS resulted in a drop in viscosity. Nanohybrids with higher ZnO content exhibited greater hydrolytic and thermal degradation.

Melt processing of biodegradable poly(butylene succinate) (PBS)—a critical review

AbstractThis review paper presents a comprehensive analysis of the melt processing of polybutylene succinate (PBS) blends and composites. PBS, a biodegradable and eco-friendly thermoplastic polyester, has garnered significant interest in sustainable material research. The paper collates and examines a wide range of studies focusing on the processability, optimization of processing parameters, and resultant mechanical properties of PBS when processed through several extrusion techniques and by injection molding. Key parameters such as melt temperature, screw speed, and mold temperature are considered for their impact on the quality and performance of the final product. The review highlights advancements in processing technologies and material modifications that enhance PBS properties, making it a viable alternative to traditional petroleum-based plastics. Furthermore, challenges and limitations in the current processing techniques are discussed, offering insights into potential areas for future research. The synthesis of findings from various studies provides a holistic understanding of the state-of-the-art in PBS processing, aiming to guide further developments in the field of biodegradable polymers. Overall, this review underscores the importance of optimized melt processing techniques in maximizing the potential of PBS as a sustainable material in diverse applications. Graphical abstract

Membrane‐Free Electrocatalytic Co‐Conversions of PBS Waste Plastics and Maleic Acid into High‐Purity Succinic Acid Solid

AbstractPlastic pollution, an increasingly serious global problem, can be addressed through the full lifecycle management of plastics, including plastics recycling as one of the most promising approaches. System design, catalyst development, and product separation are the keys in improving the economics of electrocatalytic plastics recycling. Here, a membrane‐free co‐production system was devised to produce succinic acid (SA) at both anode and cathode respectively by the co‐electrolysis of polybutylene succinate (PBS) waste plastics and biomass‐derived maleic acid (MA) for the first time. To this end, Cr3+‐Ni(OH)2 electrocatalyst featuring much enhanced 1,4‐butanediol (BDO) oxidation reaction (BOR) activity has been synthesized and the role of doped Cr has been revealed as an “electron puller” to accelerate the rate‐determining step (RDS) in the Ni2+/Ni3+ cycling. Impressively, an extra‐high SA production rate of 3.02 g h−1 and ultra‐high apparent Faraday efficiency towards SA (FEapparent=181.5 %) have been obtained. A carbon dioxide‐assisted sequential precipitation approach has been developed to produce high‐purity SA and byproduct NaHCO3 solids. Preliminary techno‐economic analysis demonstrates that the reported system is economically profitable and promising for future industrial applications.

Membrane-Free Electrocatalytic Co-Conversions of PBS Waste Plastics and Maleic Acid into High-PuritySuccinic Acid Solid.

Plastic pollution, an increasingly serious global problem, can be addressed through the full lifecycle management of plastics, including plastics recycling as one of the most promising approaches. System design, catalyst development, and product separation are the keys in improving the economics of electrocatalytic plastics recycling. Here, a membrane-free co-production system was devised to produce succinic acid (SA) at both anode and cathode respectively by the co-electrolysis of polybutylene succinate (PBS) waste plastics and biomass-derived maleic acid (MA) for the first time. To this end, Cr3+-Ni(OH)2 electrocatalyst featuring much enhanced 1,4-butanediol (BDO) oxidation reaction (BOR) activity has been synthesized and the role of doped Cr has been revealed as an "electron puller" to accelerate the rate-determining step (RDS) in the Ni2+/Ni3+ cycling. Impressively, an extra-high SA production rate of 3.02 g h-1 and ultra-high apparent Faraday efficiency towards SA (FEapparent=181.5%) have been obtained. A carbon dioxide-assisted sequential precipitation approach has been developed to produce high-purity SA and byproduct NaHCO3 solids. Preliminary techno-economic analysis demonstrates that the reported system is economically profitable and promising for future industrial applications.

Soil biota modulate the effects of microplastics on biomass and diversity of plant communities

Abstract The use of biodegradable plastics has been proposed as an alternative to mitigate the pollution problem caused by traditional non‐biodegradable plastics. However, the relative impacts of both types of microplastics on plant community productivity and diversity is not known. Moreover, it is unclear whether soil biota can differentially mediate the impacts of biodegradable and non‐biodegradable microplastics on plant communities. In this study, we investigated the effects of biodegradable and non‐biodegradable microplastics on plant community biomass production and diversity, and whether soil biota mediate these effects. We employed a fully crossed factorial design, growing six plant communities in the presence or absence of 10 individual microplastics, and in live soil versus sterilized soil. We hypothesized that: (1) Biodegradable microplastics have a less negative effect on plant community biomass production and diversity compared to non‐biodegradable microplastics. (2) Soil biota differentially mediate the effects of biodegradable and non‐biodegradable microplastics on plant community biomass production and diversity. Statistical analyses that included all 10 microplastics yielded two main findings. First, live soil ameliorated the negative effects of biodegradable microplastics on community shoot biomass. Second, the presence of microplastics, rather than their biodegradability, significantly reduced community diversity. Separate analyses of individual microplastics suggest that these patterns were driven by specific microplastics. The biodegradable microplastic polybutylene succinate (PBS) was the main driver of the pattern observed in community shoot biomass. In contrast, the biodegradable microplastic polycaprolactone (PCL) and non‐biodegradable microplastics ethylene‐vinyl acetate (EVA) and polyvinyl chloride (PVC) were the main drivers of the pattern observed in community diversity. Further analyses excluding PBS from the global models, but including the other nine microplastics, revealed no significant differences in community shoot biomass and diversity between biodegradable and non‐biodegradable microplastics in live versus sterilized soil. Synthesis and applications. Our findings suggest that biodegradable microplastics, often considered environmentally friendly, are not necessarily less harmful than non‐biodegradable microplastics to the growth and diversity of plant communities. Some individual biodegradable microplastics, such as PBS, still pose significant ecological risks to plant community structure and productivity. However, the results also suggest that soil biota may mitigate the negative effects of some biodegradable microplastics.

Biodegradation of polybutylene succinate by an extracellular esterase from Pseudomonas mendocina

An extracellular esterase (HP) with polybutylene succinate (PBS)-degrading ability was identified from Pseudomonas mendocina SA-1503. The HP also had the ability to degrade poly(3-hydroxybutyrate-co-4-hydroxybutyrate) and polycaprolactone. This HP had optimal activity at pH 9.0 and 40 °C and remained stable at pH 8.0–9.0 and temperatures of 30–40 °C. Mn2+ promoted the enzyme activity. HP could hydrolyze all p-NP fatty acid ester substrates containing even numbers of carbon atoms from C2 to C18 and had the highest catalytic activity for the p-NP C6 substrate. After 60 h of HP-catalyzed degradation, PBS films experienced a weight loss of more than 60%. Butanedioic acid, 1,4-butanediol, and a series of oligomers were detected in the degradation products of PBS by HP. Further structural analysis of HP revealed that it could be classified as a microbial esterase of α/β hydrolase superfamily and contained a conserved catalytic triad structure (Ser-148, Asp-198, and His-228) with a relatively exposed active site.

Comprehensive analysis reveals the differentiated influential mechanism of biodegradable and non-biodegradable microplastics on core microbial metabolisms and functional genes in an adsorption-biological coupling wastewater treatment system

The effects of different types of microplastics (MPs) on the wastewater treatment efficiency of an adsorption-biological coupling system were investigated. The distribution of the microbial community and metabolic pathways in the coupled system were also analyzed. Biodegradable polybutylene succinate microplastics (PBS MPs) were added to reactor A, while non-biodegradable polystyrene microplastics (PS MPs) was added to reactor B. The average chemical oxygen demand (COD) removal rates in reactor A with 0, 50, and 100 mg/L of MPs were 95.34 %, 89.13 %, and 86.08 %, respectively; the average COD removal rates in reactor B were 96.84 %, 88.43 %, and 87.02 %, respectively. The average total phosphorus (TP) removal rates in reactor A were 74.14 %, 38.94 %, and 36.45 %, respectively, while those in reactor B were 71.73 %, 39.50 %, and 33.09 %, respectively. In the two reactors, Proteobacteria had the highest relative abundance (53 %–62 %), followed by Actinobacteria. PS MPs inhibited the expression of quorum sensing genes by influencing SecA and SecY. Horizontal transfer genes illustrated that both MPs led to up-regulation of reactive oxygen species (ROS)-related functional genes. During glycolysis, the abundances of glucokinase (GLK), pyruvate kinase (PK), and phosphofructokinase (PFK) in reactor A were 0.0179 %, 0.0133 %, and 0.0387 % higher than that in reactor B, respectively. Meanwhile, in nitrogen metabolism, the abundance of key genes such as nasA (A: 40.8 % B: 37.9 %) was greater in reactor A than in reactor B.