Search

ABSTRACTThis study examines attitudes and perceptions towards biodegradable disposable products, as well as the willingness to pay for them in the southern region of Jalisco. Surveys were conducted among residents to explore their consumption patterns and the reasons influencing their purchasing decisions. The results highlight that only one in three individuals in this region shows a preference for biodegradable disposables, with a stronger inclination among women and those with higher educational levels. Despite a general interest in environmental preservation and a willingness to adopt biodegradable products, these factors were found to have no significant impact on the final purchasing decision. These findings suggest that governmental initiatives to promote the adoption of biodegradable disposables have not yet achieved significant adherence among the local population. This study provides valuable insights into current challenges in adopting sustainable practices and emphasises the need for more effective strategies to drive changes in consumer behaviour in the region.

Plastic pollution, a pervasive environmental crisis, arises from the improper disposal of non-biodegradable plastics, endangering species and ecosystems worldwide. While microplastics (MPs) have been extensively studied in various ecosystems, they have received scant attention in port environments, despite their pervasive presence. This review selected published articles conducted in ports worldwide between 2010 and 2024 to determine the concentration, accumulation characteristics, and driving factors. A total of 57 studies across 78 ports met the selection criteria, examining water, sediment, and biota in 49, 51, and 23 ports, respectively. The average concentrations of MPs in water collected by net and grab sampling, sediment, fish, and invertebrates were approximately 39.2 ± 68.4 items/m3, 4100.7 ± 5761.8 items/m3, 243.6 ± 240.2 items/kg, 26.1 ± 21.1 items/individual, and 9.4 ± 8.1 items/individual in ports worldwide, respectively. Asia and the Americas exhibited the highest concentration of MPs in ports across all media. The dominant MP morphotypes included fibers, fragments, films, foams, pellets, and spheres, with sizes frequently between 1 and 1000 μm in biota and water and between 1 and 5 mm in sediments. Port structures and the presence of rivers are key drivers of MP accumulation. MP pollution in ports poses potential ecological and health risks. Among the studied ports, 23% had MP numbers in sediment greater than the predicted no effect concentration (PNEC). The presence of MP in biota and the capability of MP to adsorb other contaminants pose a threat to human health. [ABSTRACT FROM AUTHOR]

Gamma-aminobutyric acid (GABA), which is synthesized from l -glutamic acid via glutamate decarboxylase (Gad), is used as food, supplements, and biodegradable plastics. Our previous study demonstrated an Escherichia coli mutant (ΔΔ) strain, lacking type I NADH dehydrogenase (NDH-I) and cytochrome bo 3 oxidase (Cyt bo 3), produced 7 g/L glutamic acid on MS1 glucose-minimal medium. In this study, the ΔΔ strain was used for improving GABA production. A plasmid (pMBL19- gadB ′) expressing a mutated E. coli GadB (Glu89Gln/Δ452-466), retaining activity at neutral pH, was introduced into the ΔΔ strain and its parent strain (W1485). The ΔΔ strain carrying pMBL19- gadB ′ exhibited a twofold increase in GABA production compared to the W1485 strain carrying pMBL19- gadB ′. Deleting the C-terminal (Δ471–511) of GadC antiporter in the ΔΔ strain further improved GABA yield to 1.5 g/L when cultured in MS1 glucose-minimal medium. On the other hand, a large amount of glutamic acid produced by the ΔΔ strain was not fully converted to GABA, likely due to the inhibition of GadB activity by the accumulation of acetic acid. Although there is room for improvement, these results indicate the efficacy of the ΔNDH-IΔCyt bo 3 double mutation in augmenting GABA production. [ABSTRACT FROM AUTHOR]

This comprehensive review investigates the potential of cyanobacteria, particularly nitrogen-fixing strains, in addressing global challenges pertaining to plastic pollution and carbon emissions. By analyzing the distinctive characteristics of cyanobacteria, including their minimal growth requirements, high photosynthetic efficiency, and rapid growth rates, this study elucidates their crucial role in transforming carbon sequestration, biofuel generation, and biodegradable plastic production. The investigation emphasizes cyanobacteria’s efficiency in photosynthesis, positioning them as optimal candidates for cost-effective bioplastic production with minimized land usage. Furthermore, the study explores their unconventional yet promising utilization in biodiesel production, mitigating environmental concerns such as sulfur emissions and the presence of aromatic hydrocarbons. The resulting biodiesel exhibits significant combustion potential, establishing cyanobacteria as a viable option for sustainable biofuel production. Through a comprehensive assessment of both achievements and challenges encountered during the commercialization process, this review offers valuable insights into the diverse contributions of cyanobacteria. Its objective is to provide guidance to researchers, policymakers, and industries interested in harnessing bio-inspired approaches for structural and sustainable applications, thereby advancing global efforts towards environmentally conscious plastic and biofuel production.

Abstract Pyrolytic synergistic interactions, in which the production of pyrolyzates is enhanced or inhibited, commonly occur during the co-pyrolysis of different polymeric materials, such as plastics and biomass. Although these interactions can increase the yield of desired pyrolysis products under controlled degradation conditions, the desired compounds must be separated from complex pyrolyzates and further purified. To balance these dual effects, this study was aimed at examining pyrolytic synergistic interactions during slow heating co-pyrolysis of biodegradable plastics including polylactic acid (PLA) and poly(3-hydroxybutyrate-co-3-hydroxyhexaoate) (PHBH) and petroleum-based plastics including high-density polyethylene (HDPE), polypropylene (PP), and polystyrene (PS). Comprehensive investigations based on thermogravimetric analysis, pyrolysis–gas chromatography/mass spectrometry, and evolved gas analysis-mass spectrometry revealed that PLA and PHBH decompose at lower temperatures (273–378 °C) than HDPE, PP, and PS (386–499 °C), with each polymer undergoing independent decomposition without any pyrolytic interactions. Thus, the independent pyrolysis of biodegradable plastics, such as PLA and PHBH, with common plastics, such as HDPE, PP, and PS, can theoretically be realized through temperature control, enabling the selective recovery of their pyrolyzates in different temperature ranges. Thus, pyrolytic approaches can facilitate the treatment of mixed biodegradable and common plastics.

Polyhydroxyalkanoates (PHA) are popular biopolymers due to their potential use as biodegradable thermoplastics. In this study, three aerobic sequencing batch reactors were operated identically except for their temperatures, which were set at 15 °C, 35 °C, and 48 °C. The reactors were subjected to a feast-famine feeding regime, where carbon sources are supplied intermittently, to enrich PHAaccumulating microbial consortia. The biomass was sampled for 16S rRNA gene amplicon sequencing of both DNA (during the enrichment phase) and cDNA (during the enrichment and accumulation phases). All temperatures yielded highly enriched PHA-accumulating consortia. Thermophilic communities were significantly less diverse than those at low or mesophilic temperatures. In particular, Thauera was highly adaptable, abundant, and active at all temperatures. Low temperatures resulted in reduced PHA production rates and yields. Analysis of the microbial community revealed a collapse of community diversity during low-temperature PHA accumulation, suggesting that the substrate dosing strategy was unsuccessful at low temperatures. This points to future possibilities for optimizing low-temperature PHA accumulation. [ABSTRACT FROM AUTHOR]

Biobased biodegradable materials are gaining popularity with increasing public awareness on the negative impacts of conventional plastics on the environment. There is, however, a lack of promising biobased materials suitable for various end‐use applications that are also environmentally safe. Recently, banana sap and banana fibres have been explored as a potential source of organic material as they are abundant, cost‐efficient, and environmentally friendly. In this study, two hybrid bioresins (1) banana sap maleate (BSM) and (2) banana sap maleate + banana fibre (BSMF) were developed, and their material properties and environmental suitability were examined by analysing their physicochemical characterisation and biodegradation testing. We used thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy for the physicochemical characterisation of BSMF before and after composting and measured carbon dioxide evolved during the biodegradation to calculate biodegradability. SEM analysis also showed a significant disintegration and surface degradation in BSMF compared to BSM and other control materials such as control resin and cellulose. CO2 mineralization results indicated a potential microbial bioassimilation of the materials under composting conditions. Biodegradability of the BSMF composite, as indicated by CO2 emission, was 17.6% higher than BSM and other control materials used in this study. The present study provides crucial evidence that the reinforcement of banana fibre into banana sap bioresin composite can significantly improve material properties and enhance biodegradability in the composting conditions. These results are quite promising as they show that, with some tweaking; natural materials can reduce environmental impact of composites and improve material properties for different end‐use applications and involves less exploitation of nonrenewable resources for polymer production. This study also provides an avenue to consider BSMF for carrying out our future life cycle assessment (LCA) and to compare with commercial product's LCA. In a circular economy approach, characteristics such as durability, environmental toxicity, and recyclability of such materials should be studied and optimised to reduce energy consumption and environmental impact. [ABSTRACT FROM AUTHOR]

Plastic pollution is worsening the living conditions on Earth, primarily due to the toxicity and stability of non‐biodegradable plastics (NBPs). Photocatalytic cracking of NBPs is emerging as a promising way to cleave inert C−C bonds and abstract the carbon atoms from these wastes into valuable chemicals and fuels. However, controlling these processes is a huge challenge, ascribed to the complicated reactions of various NBPs. Herein, we summarize recent advances in the CO2 and carbon‐radical‐mediated photocatalytic cracking of NBPs, with an emphasis on the pivotal intermediates. The CO2‐mediated cracking proceeded with indiscriminate C−H/C−C bond cleavage of NBPs and tandem photoreduction of CO2, while carbon‐radical‐mediated cracking was realized by the prior activation of C−H bonds for selective C−C bond cleavage of NBPs. Catalytic generation and conversion of different intermediates greatly depend on the kinds of active species and the structure of photocatalysts under irradiation. Meanwhile, the fate of a specific intermediate is compared with small molecule activation to reveal the key problems in the cracking of NBPs. Finally, the challenges and potential directions are discussed to improve the overall efficiency in the photocatalytic cracking of NBPs. [ABSTRACT FROM AUTHOR]

Plastic pollution is a problem that threatens the future of humanity, and various methods are being researched to solve it. Plastic biodegradation using microorganisms is one of these methods, and a recent study reported that plastic-degrading microorganisms activated by plasma increase the plastic decomposition rate. In contrast to microbial sterilization using low-temperature plasma, microbial activation requires a stable plasma discharge with a low electrode temperature suitable for biological samples and precise control over a narrow operating range. In this study, various plasma characteristics were evaluated using SDBD (Surface Dielectric Barrier Discharge) to establish the optimal conditions of plasma that can activate plastic-degrading microorganisms. The SDBD electrode was manufactured using low-temperature co-fired ceramic (LTCC) technology to ensure chemical resistance, minimize impurities, improve heat conduction, and consider freedom in designing the electrode metal part. Plasma stability, which is important for microbial activation, was investigated by changing the frequency and pulse width of the voltage applied to the electrode, and the degree of activation of plastic-degrading microorganisms was evaluated under each condition. The results of this study are expected to be used as basic data for research on the activation of useful microorganisms using low-temperature plasma. [ABSTRACT FROM AUTHOR]

The present study examines the use of waste cooking oil (WCO) as a substrate for medium-chain-length polyhydroxyalkanoates (mcl-PHA) production by Pseudomonas rhizophila S211. The genome analysis revealed that the S211 strain has a mcl-PHA cluster (phaC1ZC2DFI) encoding two class II PHA synthases (PhaC1 and PhaC2) separated by a PHA depolymerase (PhaZ), a transcriptional activator (PhaD) and two phasin-like proteins (PhaFI). Genomic annotation also identified a gene encoding family I.3 lipase that was able to hydrolyze plant oils and generate fatty acids as favorable carbon sources for cell growth and PHA synthesis via β-oxidation pathway. Using a three-variable Doehlert experimental design, the optimum conditions for mcl-PHA accumulation were achieved in 10% of WCO-based medium with an inoculum size of 10% and an incubation period of 48 h at 30 °C. The experimental yield of PHA from WCO was 1.8 g/L close to the predicted yield of 1.68 ± 0.14 g/L. Moreover, 1H nuclear magnetic resonance spectroscopy analysis confirmed the extracted mcl-PHA. Overall, this study describes P. rhizophila as a cell factory for biosynthesis of biodegradable plastics and proposes green and efficient approach to cooking oil waste management by decreasing the cost of mcl-PHA production, which can help reduce the dependence on petroleum-based plastics. [ABSTRACT FROM AUTHOR]

With the growing awareness of microplastics in the environment, the question of microplastics as remnants of biodegradable plastic (BDP) products is gaining momentum. BDP bags for kitchen waste collection are often certified as fully compostable as proof of industrial compostability. Frequently certification is done using under standardized laboratory conditions within 12 weeks. Composting plants often process biowaste into compost in a shorter time under inhomogeneous conditions. This study investigates the decomposition behavior of commercially available BDP bags for kitchen waste collection at an industrial composting plant within a practically realistic time frame of 6 weeks. The research determines the decomposition behavior under practice conditions. Four bag types, two made from thermoplastic starch (TPS) blends and two from polylactic acid (PLA) blends underwent composting. The decomposition was evaluated by examining the remaining macro- (> 8 mm), meso- (2-8 mm), and microparticles (1-2 mm) in the compost with different methods. After 6 weeks, the mass-based decomposition rate of TPS blend bags exceeded 95%. In contrast, PLA blend bags failed to reach a decomposition rate of 90%. The study did not depict very small particles <1 mm. However, they are present. The study findings indicate that composting time and conditions, inhomogeneities, as well as the bag type are crucial factors influencing the decomposition of BDP bags. Concerns are raised about the usefulness of DIN 13432 as certification scheme for industrial conditions. [ABSTRACT FROM AUTHOR]

Lignocellulose is a major biopolymer in plant biomass with a complex structure and composition. It consists of a significant amount of high molecular aromatic compounds, particularly vanillin, syringeal, ferulic acid, and muconic acid, that could be converted into intracellular metabolites such as polyhydroxyalkanoates (PHA) and hydroxybutyrate (PHB), a key component of bioplastic production. Several pre-treatment methods were utilized to release monosaccharides, which are the precursors of the relevant pathway. The consolidated bioprocessing of lignocellulose-capable microbes for biomass depolymerization was discussed in this study. Carbon can be stored in a variety of forms, including PHAs, PHBs, wax esters, and triacylglycerides. From a biotechnology standpoint, these compounds are quite adaptable due to their precursors' utilization of hydrogen energy. This study lays the groundwork for the idea of lignocellulose valorization into value-added products through several significant dominant pathways. [ABSTRACT FROM AUTHOR]

Amid the current environmental crisis caused by plastic accumulation, one of the proposed solutions to manage this problem is using biodegradable polymers. However, the impact of adding biodegradable polymers to the well-established circular economy of recyclable polymers, such as HDPE, has not been fully considered. Therefore, there is a need to reconsider the way we consume, dispose of, and manage biodegradable polymers after use. This study evaluates the effect of varying the contents of a biodegradable polymer, taking poly(lactic acid) (PLA) as a model biodegradable polymer, on the thermal and mechanical properties of HDPE. The study highlights the importance of identifying and disposing of biodegradable polymers to avoid mixtures with HDPE, in order not to affect mechanical performance when considering reprocessing and a new life cycle of this conventional polymer. [ABSTRACT FROM AUTHOR]

This research improves the strength of plastic using avocado seed starch and PLA. The effect of blending avocado seed starch and PLA was optimized using the RSM approach by using two variables: water absorption and biodegradability. Mixing them using RSM gave the best result: 1.8 g of starch and 3 g of PLA. Degradable plastic has a tensile strength of 10.1 MPa, elongation at a break of 85.8%, and a Young's modulus of 190 MPa. Infrared spectroscopy showed that the plastic had a -OH bond at 3273.20 cm−1, 3502.73 cm−1, and 3647.39 cm−1, a CH2 bond at 2953.52 cm−1, 2945.30 cm−1, and 2902.87 cm−1, a C=C bond at 1631.78 cm−1, and a C-O bond at 1741.72 cm−1. The plastic decomposed in the soil. It was organic and hydrophilic. Thermal tests demonstrated that the plastic can withstand heat well, losing weight at 356.86 °C to 413.64 °C, forming crystals and plastic melts at 159.10 °C—the same as PLA. In the melt flow test, the sample melted before measurement, and was therefore not measurable—process conditions affected it. A water absorption of 5.763% and biodegradation rate of 37.988% were found when the samples were decomposed for 12 days. The starch and PLA fused in the morphology analysis to form a smooth surface. The RSM value was close to 1. The RSM gave the best process parameters. [ABSTRACT FROM AUTHOR]

Proper waste sorting is crucial for biodegradable plastics (BDPs) recycling, whose global production is increasing dynamically. BDPs can be sorted using near-infrared (NIR) sorting, but little research is available about the effect of surface contamination on their NIR spectrum, which affects their sortability. As BDPs are often heavily contaminated with food waste, understanding the effect of surface contamination is necessary. This paper reports on a study on the influence of artificially induced surface contamination using food waste and contamination from packaging waste, biowaste, and residual waste on the BDP spectra. In artificially contaminated samples, the absorption bands (ADs) changed due to the presence of moisture (1352–1424 nm) and fatty acids (1223 nm). In real-world contaminated samples, biowaste samples were most affected by contamination followed by residual waste, both having altered ADs at 1352–1424 nm (moisture). The packaging waste-contaminated sample spectra closely followed those of clean and washed samples, with a change in the intensity of ADs. Accordingly, two approaches could be followed in sorting: (i) affected wavelength ranges could be omitted, or (ii) contaminated samples could be used for optimizing the NIR database. Thus, surface contamination affected the spectra, and knowing the wavelength ranges containing this effect could be used to optimize the NIR database and improve BDP sorting. [ABSTRACT FROM AUTHOR]

Biodegradable biobased polymers derived from biomass (such as plant, animal, marine, or forestry material) show promise in replacing conventional petrochemical polymers. Research and development have been conducted for decades on potential biodegradable biobased polymers such as polylactic acid (PLA), polyhydroxyalkanoates (PHAs), and succinate polymers. These materials have been evaluated for practicality, cost, and production capabilities as limiting factors in commercialization; however, challenges, such as the environmental limitations on the biodegradation rates for biodegradable biobased polymer, need to be addressed. This review provides a history and overview of the current development in the synthesis process and properties of biodegradable biobased polymers, along with a techno-commercial analysis and discussion on the environmental impacts of biodegradable biobased polymers. Specifically, the techno-commercial analysis focuses on the commercial potential, financial assessment, and life-cycle assessment of these materials, as well as government initiatives to facilitate the transition towards biodegradable biobased polymers. Lastly, the environmental assessment focuses on the current challenges with biodegradation and methods of improving the recycling process and reusability of biodegradable biobased polymers. [ABSTRACT FROM AUTHOR]

The ever-increasing presence of micropollutants necessitates the development of environmentally friendly bioremediation strategies. Inspired by the remarkable versatility and potent catalytic activities of microbial enzymes, researchers are exploring their application as biocatalysts for innovative environmental cleanup solutions. Microbial enzymes offer remarkable substrate specificity, biodegradability, and the capacity to degrade a wide array of pollutants, positioning them as powerful tools for bioremediation. However, practical applications are often hindered by limitations in enzyme stability and reusability. Enzyme immobilization techniques have emerged as transformative strategies, enhancing enzyme stability and reusability by anchoring them onto inert or activated supports. These improvements lead to more efficient pollutant degradation and cost-effective bioremediation processes. This review delves into the diverse immobilization methods, showcasing their success in degrading various environmental pollutants, including pharmaceuticals, dyes, pesticides, microplastics, and industrial chemicals. By highlighting the transformative potential of microbial immobilized enzyme biocatalysts, this review underscores their significance in achieving a cleaner and more sustainable future through the mitigation of micropollutant contamination. Additionally, future research directions in areas such as enzyme engineering and machine learning hold immense promise for further broadening the capabilities and optimizing the applications of immobilized enzymes in environmental cleanup. [ABSTRACT FROM AUTHOR]

Plastic packaging materials have caused significant environmental issues because they are nonrenewable and nonbiodegradable. Wax‐emulsified films from biomaterials, on the other hand, are renewable and biodegradable, making them promising packaging alternatives. The development of bioactive wax‐emulsified films (BWEFs) with antimicrobial and antioxidant properties has been a topic of extensive research. In this review, we provide an overview of wax emulsification, BWEF processing, and applications. BWEF contains several bioactive agents such as tannins, flavonoids, phenolic acids, and carotenes. The addition of emulsified wax and active agents to films not only enhances their antimicrobial and antioxidant properties but also reduces their hydrophilicity. Other reagents have been added to BWEF partially to increase hydrophobicity and mainly to improve mechanical properties. BWEFs prolong food shelf life, monitor wound healing, and control drug delivery. We have identified some research challenges that need to be solved to make BWEFs industrially attractive. [ABSTRACT FROM AUTHOR]

Microplastics have become a pressing environmental issue due to their widespread presence in our ecosystems. Among various plastic components, polyethylene (PE) is a prevalent and persistent contaminant. Hydrothermal gasification (HTG), a promising technology for converting PE into syngas, holds great promise for mitigating the microplastic problem. In this study, we employ ReaxFF molecular dynamics simulations to investigate the HTG process of PE, shedding light on the intricate relationships between temperature, water content, carbon conversion efficiency, and product distributions. The results reveal that hydrothermal gasification of PE is a complex process involving multiple reaction pathways. Consistently with experimental findings, the calculations indicate that the gas phase exhibits a substantial hydrogen fraction, reaching up to 70%. Interestingly, our simulations reveal a dual role of water content in the HTG process. On one hand, water enhances hydrogen production by promoting the gas formation. On the other hand, it elevates the activation energy required for PE decomposition. Depending on the water content, the calculated activation energies range from 176 to 268 kJ/mol, which are significantly lower than those reported for thermal gasification (TG). This suggests that HTG may be a more efficient route for PE conversion. Furthermore, this study highlights the importance of optimizing both temperature and water content in HTG systems to achieve high yields of hydrogen-rich syngas. The results obtained from our ReaxFF MD simulations demonstrate the robustness of this computational methodology in elucidating complex chemical reactions under extreme conditions. Our findings offer critical insights into the design of advanced waste management strategies for microplastics and contribute to the development of sustainable practices for resource recovery. This work underscores the potential of HTG as a key technology for addressing the global challenge of plastic pollution. [ABSTRACT FROM AUTHOR]

Pyrolysis of waste plastics can produce a product mixture with a high concentration of olefins (>50 wt%). The olefins, as building blocks in the petroleum industry, are potential precursors for valuable commodity chemicals with higher values (>$2000 per ton). In this work, we produce aldehydes by hydroformylation of the olefins present in pyrolysis oil from colored post-consumer recycled high-density polyethylene (PCR-HDPE). The obtained aldehydes in the oil are then converted into aliphatic amines via reductive amination with a Ru/C catalyst. The aminated oil was characterized by multiple analytical chemistry techniques including elemental analysis, nuclear magnetic resonance spectroscopy, high-resolution liquid chromatography-mass spectrometry, and gas chromatography-mass spectrometry with a Polyarc flame ionization detector. The concentration of metals in the PCR-HDPE and oil changes during the tandem processes, showing limited effects of these elements (e.g., Al, Ca, Fe, Mg, Ti, Zn) on hydroformylation and reductive amination. Additionally, we demonstrated that reductive amination of aldehydes with varied carbon numbers and branching properties can be achieved in the presence of a complex mixture, including paraffins and aromatics. The results indicate that waste plastics have the potential to serve as a renewable source for mono and di aliphatic amines, thereby diminishing reliance on fossil feedstocks as the current primary amine source. [ABSTRACT FROM AUTHOR]

Over 79 % of 6.3 billion tonnes of plastics produced from 1950 to 2015 have been disposed in landfills or found their way to the oceans, where they will reside for up to hundreds of years before being decomposed bringing upon significant dangers to our health and ecosystems. Plastic photoreforming offers an appealing alternative by using solar energy and water to transform plastic waste into value‐added chemical commodities, while simultaneously producing green hydrogen via the hydrogen evolution reaction. This review aims to provide an overview of the underlying principles of emerging plastic photoreforming technologies, highlight the challenges associated with experimental protocols and performance assessments, discuss recent global breakthroughs on the photoreforming of plastics, and propose perspectives for future research. A critical assessment of current plastic photoreforming studies shows a lack of standardised conditions, hindering comparison amongst photocatalyst performance. Guidelines to establish a more accurate evaluation of materials and systems are proposed, with the aim to facilitate the translation of promising fundamental discovery in photocatalysts design. [ABSTRACT FROM AUTHOR]

The prevalent use of unsustainable polymers in current X‐ray scintillators poses a significant environmental concern. The advancement of biodegradable X‐ray scintillators holds promise in mitigating escalating environmental issues tied to electronic or medical waste and carbon footprints. Herein, a biodegradable and flexible X‐ray scintillation film is presented employing lead‐free 0D Cs3Cu2I5 perovskite nanoparticles integrated into densified‐delignified wood (Cs3Cu2I5@D‐Wood). The Cs3Cu2I5@D‐Wood film demonstrates precise and detailed X‐ray imaging capabilities, achieving a high spatial resolution of 10 line pairs per millimeter (lp·mm−1). To minimize the environmental impact associated with disposal, metal and halide ions (e.g., Cs+, Cu+, I−) from Cs3Cu2I5@D‐Wood can be easily retrieved by a simple solvent extraction process. The approach showcases the potential of biodegradable wood‐based X‐ray scintillation screens as alternatives to conventional, plastic‐based screens. This offers a significant contribution to environmental sustainability by reducing electronic or medical waste. [ABSTRACT FROM AUTHOR]

In recent years, there has been increasing interest in developing novel materials based on natural biopolymers as a renewable alternative to petroleum-based plastics. The availability of proteins derived from agricultural by-products, along with their favourable properties, has fostered a renewed interest in protein-based materials, promoting research in innovative technologies. In this study, we propose the use of rapeseed protein-rich meal as the main ingredient for the preparation of novel sustainable materials combining excellent environmental properties such as biodegradability and renewability. The application of sustainable products in the present high-tech society requires the modification of the basic native properties of these natural compounds. The original route proposed in this paper consists of preparation via the compression moulding of flexible biomaterials stabilized by crosslinkers/chain extenders. An investigation of the effects of different denaturing and disulfide bond reducing agents, crosslinkers, and preparation conditions on the material mechanical behaviour demonstrated that the novel materials have appreciable strength and stiffness. The results show the potential of utilizing full meal from vegetable by-products to prepare protein-based materials with guaranteed ecofriendly characteristics and mechanical properties adequate for specific structural applications. [ABSTRACT FROM AUTHOR]

Petroleum‐based plastics levy significant environmental and economic costs that can be alleviated with sustainably sourced, biodegradable, and bio‐based polymers such as polyhydroxyalkanoates (PHAs). However, industrial‐scale production of PHAs faces barriers stemming from insufficient product yields and high costs. To address these challenges, we must look beyond the current suite of microbes for PHA production and investigate non‐model organisms with versatile metabolisms. In that vein, we assessed PHA production by the photosynthetic purple non‐sulfur bacteria (PNSB) Rhodomicrobium vannielii and Rhodomicrobium udaipurense. We show that both species accumulate PHA across photo‐heterotrophic, photo‐hydrogenotrophic, photo‐ferrotrophic, and photo‐electrotrophic growth conditions, with either ammonium chloride (NH4Cl) or dinitrogen gas (N2) as nitrogen sources. Our data indicate that nitrogen source plays a significant role in dictating PHA synthesis, with N2 fixation promoting PHA production during photoheterotrophy and photoelectrotrophy but inhibiting production during photohydrogenotrophy and photoferrotrophy. We observed the highest PHA titres (up to 44.08 mg/L, or 43.61% cell dry weight) when cells were grown photoheterotrophically on sodium butyrate with N2, while production was at its lowest during photoelectrotrophy (as low as 0.04 mg/L, or 0.16% cell dry weight). We also find that photohydrogenotrophically grown cells supplemented with NH4Cl exhibit the highest electron yields – up to 58.89% – while photoheterotrophy demonstrated the lowest (0.27%–1.39%). Finally, we highlight superior electron conversion and PHA production compared to a related PNSB, Rhodopseudomonas palustris TIE‐1. This study illustrates the value of studying non‐model organisms like Rhodomicrobium for sustainable PHA production and indicates future directions for exploring PNSB metabolisms. [ABSTRACT FROM AUTHOR]

Microplastics have been recently detected in many environmental media and living organisms, yet their transfer and toxicity to humans are poorly known. Here, we review microplastic transfer in the food chain with focus on microplastic pollution sources, methods to analyze microplastics in food, health impact of food-related microplastic exposure, and remediation of microplastic pollution. Microplastic pollution sources include seafood, food additives, packaging materials, and agricultural and industrial products. Remediation techniques comprise the use of microbial enzymes and biofilms. Microplastic detection methods in food rely on separation and quantification by optical detection, scanning electron micrography, and Fourier-transform infrared spectroscopy. Human health impact following microplastic ingestion include cancers, organ and respiration damage, and reproductive impairments. Overall, microplastic toxicity is mainly due to their ability to enter the metabolism, adsorption into the circulatory system for translocation, and difficulty, if not impossibility, of excretion. [ABSTRACT FROM AUTHOR]

Bioplastics appear as an alternative to fossil fuel-derived plastics because bioplastics are carbon neutral and often biodegradable, thus potentially solving the issues of plastic pollution and climate change. In particular, polylactic acid is a substitute for traditional petrochemical-based polymers. Here, we review polylactic acid production with focus on surface modification and integration of bioactive compounds. Surface can be modified by chemical treatment, photografting, surface entrapment, plasma treatment, and coating. Bioactive compounds can be incorporated by encapsulation, impregnation, melt blending, solvent casting, electrospinning, and in situ polymerization. Biomedical and packaging applications are discussed. [ABSTRACT FROM AUTHOR]

Biopolymers are highly desirable alternatives to petrochemical-based plastics owing to their biodegradable nature. The production of bioplastics, such as polyhydroxyalkanoates (PHAs), has been widely reported using various bacterial cultures with substrates ranging from pure to biowaste-derived sugars. However, large-scale production and economic feasibility are major limiting factors. Now, using algal biomass for PHA production offers a potential solution to these challenges with a significant environmental benefit. Algae, with their unique ability to utilize carbon dioxide as a greenhouse gas (GHG) and wastewater as feed for growth, can produce value-added products in the process and, thereby, play a crucial role in promoting environmental sustainability. The sugar recovery efficiency from algal biomass is highly variable depending on pretreatment procedures due to inherent compositional variability among their cell walls. Additionally, the yields, composition, and properties of synthesized PHA vary significantly among various microbial PHA producers from algal-derived sugars. Therefore, the microalgal biomass pretreatments and synthesis of PHA copolymers still require considerable investigation to develop an efficient commercial-scale process. This review provides an overview of the microbial potential for PHA production from algal biomass and discusses strategies to enhance PHA production and its properties, focusing on managing GHGs and promoting a sustainable future. [ABSTRACT FROM AUTHOR]

Plastics have accumulated in open environments, such as oceans, rivers, and land, for centuries, but their effect has been of concern for only decades. Plastic pollution is a global challenge at the forefront of public awareness worldwide due to its negative effects on ecological systems, animals, human health, and national economies. Therefore, interest has increased regarding specific circular economies for the development of plastic production and the investigation of green technologies for plastic degradation after use on an appropriate timescale. Moreover, biodegradable plastics have been found to contain potential new hazards compared with conventional plastics due to the physicochemical properties of the polymers involved. Recently, plastic biodegradation was defined as microbial conversion using functional microorganisms and their enzymatic systems. This is a promising strategy for depolymerizing organic components into carbon dioxide, methane, water, new biomass, and other higher value bioproducts under both oxic and anoxic conditions. This study reviews microplastic pollution, the negative consequences of plastic use, and the current technologies used for plastic degradation and biodegradation mediated by microorganisms with their drawbacks; in particular, the important and questionable role of extremophilic multi-enzyme-producing bacteria in synergistic systems of plastic decomposition is discussed. This study emphasizes the key points for enhancing the plastic degradation process using extremophiles, such as cell hydrophobicity, amyloid protein, and other relevant factors. Bioprospecting for novel mechanisms with unknown information about the bioproducts produced during the plastic degradation process is also mentioned in this review with the significant goals of CO2 evolution and increasing H2/CH4 production in the future. Based on the potential factors that were analyzed, there may be new ideas for in vitro isolation techniques for unculturable/multiple-enzyme-producing bacteria and extremophiles from various polluted environments. [ABSTRACT FROM AUTHOR]

The fabrication of ultra-tough biodegradable nanocomposite films with antibacterial activity and antioxidant properties remains a huge challenge. Herein, we developed a super-tough antibacterial biodegradable poly(vinyl alcohol) (PVA) nanocomposite film by simply introducing highly effective antibacterial agent PDA@LS-Ag into PVA matrix. The antibacterial agent PDA@LS-Ag was synthesized from the mussel-inspired polydopamine (PDA) and green biomass sodium lignosulfonate (LS) via a facile microwave-assisted reduction strategy, in which PDA played the role of reducing agent and LS performed as the dispersant. The tensile strength of the PVA nanocomposite film with 5 wt% addition of PDA@LS-Ag reached up to 131.7 MPa, which was far higher than most of engineering plastics. The excellent mechanical performance was resulted from the synergistic effect of the unique nanoscale phase-separation structure and the dense hydrogen bonds between the PDA@LS-Ag nanoparticles and PVA matrix. Owing to the existence of silver nanoparticles and rich phenolic hydroxyl groups, the PDA@LS-Ag nanoparticles also endued the composite film with good antibacterial activity, outstanding antioxidant activity, and UV-shielding properties. As the biomass LS, PDA, and the PVA matrix are all biodegradable, this work provides a feasible way for preparing highly strong and super-tough biodegradable nanocomposite films with antibacterial and antioxidant properties. [ABSTRACT FROM AUTHOR]

The utilization of biodegradable hydrogels based on natural polysaccharides in the agricultural and biomedical sectors is anticipated to be a growing field of interest. Due to increasing environmental pollution, the current global goal is to synthesize sustainable materials based on natural polysaccharides to conserve natural resources for the future. In this study, we synthesized an amla-based hydrogel, denoted as AL-g-poly(MAA), using the graft-free radical polymerization method. Methacrylic acid (MAA) was employed as the monomer, N,N′-methylenebisacrylamide (MBA) served as the crosslinker, and ammonium persulfate (APS) acted as the initiator. The synthesized hydrogel, AL-g-poly(MAA), underwent optimization by adjusting seven parameters: initiator, solvent, time, monomer, power, pH, and crosslinker, to achieve the highest swelling percentage. The optimized values were as follows: solvent: 10 ml, time: 150 s, monomer: 0.039 mol/L, power: 60%, pH: 7, and crosslinker: 0.0648 mol/L. The cross-linking process was confirmed through Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and thermal gravimetric analysis (TGA) techniques. The swelling behavior of the synthesized hydrogels was determined in saline solutions with varying ionic strengths and concentrations, revealing maximum swelling in solutions with lower ionic strengths and concentrations. Additionally, the density and porosity of the hydrogels were examined. The biodegradability of AL-g-poly(MAA) was tested through soil burial and vermicomposting experiments, demonstrating its significant potential for agriculture applications. Furthermore, both the backbone and the synthesized hydrogel were evaluated for antibacterial activity against four bacterial strains (Burkholderia gladioli, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus cereus), revealing strong potential as an antimicrobial agent and therefore having applications in the biomedical field. The mechanism underlying the inhibitory effect of synthesized AL-g-poly(MAA) hydrogel on bacterial cell membranes is also discussed. [ABSTRACT FROM AUTHOR]

Starch-based thermoplastic polymer is a biopolymer that is being widely explored as a replacement for conventional polymers. Since thermoplastic starch suffers from mechanical defects, certain mechanical and thermal properties of starch-based polymers can be improved by incorporating fillers or reinforcements derived mainly from natural substances. This article reports the preparation, physicochemical, and mechanical characterization and biodegradation of starch-based bioplastics extracted from potato (Solanum tuberosum) peels using glycerol (G) as plasticizer and reinforced with carob powder, a readily growing plant in Mediterranean climates. The present study investigates the effect of incorporating different proportions (0, 2, 5, 10, and 15 wt.%) of carob powder (Cb) in the films thus prepared. These biopolymer films were fully characterized using analytical techniques including Fourier transform infrared spectroscopy with attenuated total reflection (FTIR/ATR), thermogravimetric analysis (TGA/DTG), X-ray diffraction (XRD), optical microscopy (OM), Scanning electron microscopy (SEM), mechanical evaluations, and biodegradability assessments. The biodegradability of the obtained bioplastic samples was evaluated. Scanning electron microscopy (SEM) revealed strong interfacial adhesion between the constituent filler and the polymer matrix. [ABSTRACT FROM AUTHOR]

Context: Poly(butylene adipate-co-terephthalate) (PBAT) is a biodegradable plastic. It was introduced to the plastics market in 1998 and since then has been widely used around the world. The main idea of this research is to perform quantum chemical calculations to study the potential toxicity of PBAT and its degradation products. We analyzed the electron transfer capacity to determine its potential toxicity. We found that biodegradable products formed with benzene rings are as good electron acceptors as PBAT and OOH•. Our results indicate that the biodegradation products are potentially as toxic as PBAT. This might explain why biodegradation products alter the photosynthetic system of plants and inhibit their growth. From this and other previous investigations, we can think that biodegradable plastics could represent a potential environmental risk. Methods: All DFT computations were performed using the Gaussian16 at M062x/6–311 + g(2d,p) level of theory without symmetry constraints. Electro-donating (ω-) and electro-accepting (ω +) powers were used as response functions. [ABSTRACT FROM AUTHOR]

Poly(butylene‐adipate‐co‐terephthalate) (PBAT) is recognized for its advantages as a biodegradable thermoplastic polyester. However, its application is often limited due to low strength and poor processability. In contrast, poly(4‐hydroxybutyrate) (P4HB) emerges as a fully biodegradable polyester characterized by high strength, excellent toughness, and facile processing. In this study, P4HB was employed to reinforce PBAT, and glycidyl methacrylate grafted onto poly(4‐hydroxybutyrate) (P4HB‐g‐GMA) was introduced as an effective compatibilizer to address their inherent incompatibility. The study explored the influence of P4HB‐g‐GMA content on the mechanical, thermal, morphological, and rheological properties of the blends. The findings revealed that P4HB‐g‐GMA significantly enhanced the compatibility, mechanical properties, and melt strength of PBAT/P4HB blends. Furthermore, various PBAT/P4HB foams were prepared through a batch foaming process, employing supercritical CO2 as a physical foaming agent. The volume expansion ratio and cell size of PBAT/P4HB foams increased with higher levels of the compatibilizer. [ABSTRACT FROM AUTHOR]

Large amounts of plastic waste are daily generated, becoming a global issue that needs to be addressed. Thus, new recycling alternatives have been explored, such as the depolymerization of poly(ethylene terephthalate) waste (wPET). These reactions can lead to the formation of oligomers and monomers, which can then be employed in new synthetic processes. The aim of this work is to use the products of the chemical recycling of wPET on the synthesis of hydrogels and evaluate the capacity of these materials to adsorb dyes aiming a wastewater treatment. The depolymerizations were done through glycerolysis reactions catalyzed by zinc (II) acetate under microwave radiation. Afterwards, the obtained oil was crosslinked with citric acid (CA) under tin (II) chloride catalysis to obtain the hydrogels. The water uptake capacity of the hydrogels ranged from 310% to 1442%, depending on the CA content. When placed in an indigo carmine solution, the hydrogels showed high adsorption capacity, removing up to 97% of the dye. The kinetic study revealed a physicochemical mechanism for the removal process, corroborated by Temkin isotherms. These results indicate that the chemical recycling of PET via glycerolysis is a viable alternative for producing hydrogels, reducing plastic waste while creating new tools for wastewater treatment. [ABSTRACT FROM AUTHOR]

Polymeric methylene diphenyl isocyanate (pMDI) was used as a reactive compatibilizer to improve the mechanical properties of the PBAT/EVOH blend. Initially, pMDI was blended with pure polymers. Adding pMDI led to a 10‐fold rise in the viscosity of PBAT/pMDI compared to pure PBAT, with an enhancement in tensile properties, attributed to pMDI's chain‐extending effect in the PBAT phase. Conversely, a reduction in the elongation at the break of EVOH/pMDI indicated a cross‐linking role for pMDI in the EVOH phase. Notably, the blend with 1 wt% of pMDI showed a high tensile strength of 38 MPa by route II, much above 13.5 MPa for the one prepared by route I, and 14 MPa for the blank PBAT/EVOH blend without pMDI. Fourier transform infrared (FTIR) spectra, FE‐SEM images, and dynamic mechanical thermal analysis (DMTA) results confirmed the occurrence of effective reactions in route II. Modification of the blend with pMDI decreased the crystallinity of EVOH, the size of EVOH droplets, and the oxygen transmission rate (OTR) of the blends. However, an increase in the pMDI content above 0.5 wt% decreased OTR. Therefore, the modified blends of PBAT/EVOH with pMDI can be used as an efficient compatibilizer or adhesive layer in PBAT/EVOH blends or multilayer films for agricultural or food packaging applications. [ABSTRACT FROM AUTHOR]

Polylactic acid (PLA) is a high-modulus, high-strength biodegradable thermoplastic polyester used in the packaging, textile and medical industries. Conventional plasticizers are usually non-biodegradable, the study used low molecular polyhexanediol succinate (PHS) blended with poly (L-lactic acid) (PLLA) to obtain a fully degradable system. The compatibility, crystallization and mechanical properties of the blended system were investigated by differential scanning calorimetry, polarizing microscope and universal testing machine. The results show that the crystallinity of PLLA/PHS ratios of 100/0, 95/5, 90/10, 85/15, and 80/20 were 7.5%, 8.7%, 11.5%, 14.1%, and 14.2%, respectively. The crystallinity of the blends increased with increasing PHS content, indicating that PHS successfully promoted PLLA crystallization. In addition, the crystallization rate of 80/20 was increased 10-fold and the semi-crystallization time was halved compared to pure PLLA. The elongation at break of the blends increased from less than 10% for pure PLLA to about 60% (PHS content 20%), with a slight decrease in strength and modulus. The elastic modulus of the blends decreased continuously with the increase of the PHS content, from 2.25 GPa for pure PLLA to 1.86 GPa at 20% PHS content. [ABSTRACT FROM AUTHOR]

Nowadays, there is a rising interest in the packaging industry regarding more environment‐friendly (i.e. biodegradable and/or compostable) polymer‐based solutions, especially for film blowing applications. However, replacing traditional, fossil resource‐based polymers typically used for such applications is not an easy task, since the more environment‐friendly solutions must have adequate features in terms of processability and final properties. In this work, three commercial biodegradable (and, at least partially, biobased) polymers were investigated by a preliminary rheological and mechanical analysis, in order to perform film manufacturing experiments in laboratory equipment. Furthermore, oxygen and water vapour barrier properties were studied by permeability measurements. The investigation was ultimately performed on films produced in industrial equipment, and the results were compared to those for a typical, standard polypropylene (PP) film used in flexible packaging applications. It was found that the mechanical properties were adequate (in some cases, even up to 25–30% higher than for the PP counterpart), as well as oxygen permeability. On the other hand, water permeability was significantly higher than that of PP films, and this should be taken into account in cases where high water vapour barrier properties are required. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

The impact of ultrasound‐assisted fermentation using Lactobacillus species was investigated, for enhanced lactic acid production. The different ultrasound frequencies of 20, 30, and 40 Hz, with time intervals of 3, 4, and 5 min, and with corn steep liquor concentrations of 1%–3% were examined using response surface methodology‐Box–Behnken design. The growth of lactic acid production was modeled by Contois model (linear) and Baranyi–Roberts model (nonlinear), assessing the suitability of Lactobacillus paracasei, Lactobacillus plantarum, and Lactobacillus acidophilus for industrial processes. At 34 h, the maximal lactic acid generation of L. paracasei, L. plantarum, and L. acidophilus was 85.2%, 82.1%, and 79.4%, respectively. The R2, μmax, and Ks values for L. paracasei and L. plantarum were found to be 0.9158, 0.574 h−1, 54.27 g/L and 0.9426, 0.294 h−1, 22.66 g/L, respectively, using Contois model. The observed R2 values of Baranyi–Roberts model for the strains L. acidophilus, L. paracasei, and L. plantarum were 0.9947, 0.9954, and 0.9998, respectively. Practical Applications: Lactic acid is crucial in the fermentation process for products like yogurt, sauerkraut, kimchi, and pickles, enhancing flavor, texture, and shelf life. As a precursor to biodegradable plastics, lactic acid contributes to the development of sustainable packaging materials and environmentally friendly alternatives to traditional plastics. Utilizing waste corn steep liquor (CSL) as a growth medium presents a sustainable and cost‐effective solution for lactic acid production, capitalizing on its rich nutrient profile to enhance microbial growth. As a byproduct of corn wet milling, using CSL for fermentation processes promotes waste valorization and contributes to a circular economy. The optimization of fermentation conditions using the Box–Behnken design ensures maximum yield and efficiency by systematically evaluating the effects of key process variables. Integrating advanced growth curve models like the Contois and Baranyi models further refines the understanding and prediction of microbial dynamics, enabling precise control over the fermentation process. This comprehensive approach not only promotes the efficient use of industrial by‐products but also advances the development of environmentally friendly and economically viable bioprocesses. [ABSTRACT FROM AUTHOR]

Accumulation of polyethylene terephthalate (PET) polyester in ecosystems across the globe is a major pollution of concern. Microbial degradation recently generated novel insights into the biodegradation of varieties of plastics. In this study, a PET degrading bacterium Brucella intermedia IITR130 was isolated from a contaminated lake ecosystem at Pallikaranai, Chennai, India. Incubation of the bacterium along with the PET sheet (0.1 mm thickness) for 60 days resulted in 26.06% degradation, indicating a half-life of 137.8 days. Considerable changes in the surface morphology of the PET sheet were found as holes, pits, and cracks on incubation with strain IITR130, as revealed by scanning electron microscopy (SEM). After bacterial treatment of PET, the formation of new functional groups, most notably in the area of 3326 cm−1 suggestive of O–H stretch, leading to carboxylic acid and alcohol as products were suggested by fourier transform infrared (FTIR) analysis. Monomethyl terephthalate (MMT) and terephthalic acid (TPA) were identified by gas chromatography–mass spectrometry (GC–MS) analysis as PET degradation metabolites. Tributyrin clearance assay confirmed the presence of a lipase/esterase enzyme in the strain IITR130. In this study, a degradation pathway for PET by an isolated and identified bacterium Brucella intermedia IITR130 was characterized in detail. [ABSTRACT FROM AUTHOR]

Environmental pollution caused by petrochemical hydrocarbons (HC) and plastic waste is a pressing global challenge. However, there is a promising solution in the form of bacteria that possess the ability to degrade HC, making them valuable tools for remediating contaminated environments and effluents. Moreover, some of these bacteria offer far-reaching potential beyond bioremediation, as they can also be utilized to produce polyhydroxyalkanoates (PHAs), a common type of bioplastics. The accumulation of PHAs in bacterial cells is facilitated in environments with high C/N or C/P ratio, which are often found in HC-contaminated environments and effluents. Consequently, some HC-degrading bacteria can be employed to simultaneously produce PHAs and conduct biodegradation processes. Although bacterial bioplastic production has been thoroughly studied, production costs are still too high compared to petroleum-derived plastics. This article aims to provide a comprehensive review of recent scientific advancements concerning the capacity of HC-degrading bacteria to produce PHAs. It will delve into the microbial strains involved and the types of bioplastics generated, as well as the primary pathways for HC biodegradation and PHAs production. In essence, we propose the potential utilization of HC-degrading bacteria as a versatile tool to tackle two major environmental challenges: HC pollution and the accumulation of plastic waste. Through a comprehensive analysis of strengths and weaknesses in this aspect, this review aims to pave the way for future research in this area, with the goal of facilitating and promoting investigation in a field where obtaining PHAs from HC remains a costly and challenging process. [ABSTRACT FROM AUTHOR]

Plastic pollution has become a global problem since the extensive use of plastic in industries such as packaging, electronics, manufacturing and construction, healthcare, transportation, and others. This has resulted in an environmental burden that is continually growing, which has inspired many scientists as well as environmentalists to come up with creative solutions to deal with this problem. Numerous studies have been reviewed to determine practical, affordable, and environmentally friendly solutions to regulate plastic waste by leveraging microbes' innate abilities to naturally decompose polymers. Enzymatic breakdown of plastics has been proposed to serve this goal since the discovery of enzymes from microbial sources that truly interact with plastic in its naturalistic environment and because it is a much faster and more effective method than others. The scope of diverse microbes and associated enzymes in polymer breakdown is highlighted in the current review. The use of co-cultures or microbial consortium-based techniques for the improved breakdown of plastic products and the generation of high-value end products that may be utilized as prototypes of bioenergy sources is highlighted. The review also offers a thorough overview of the developments in the microbiological and enzymatic biological degradation of plastics, as well as several elements that impact this process for the survival of our planet. [ABSTRACT FROM AUTHOR]

The escalating worldwide concerns over the difficult degradation and pollution of plastic and its associated environmental and health risks have amplified the urgent need to develop biodegradable alternatives to traditional plastics. Polyhydroxyalkanoates (PHAs) have emerged as a promising class of biopolymers that offer a sustainable solution. Their commercial success in various applications has highlighted PHAs' potential to mitigate environmental impact. Critical to the economic feasibility of PHA production is the optimization of downstream processing methods, crucial for scaling operations from pilot to industrial scales. This paper reviews two decades of pilot-scale studies on PHA extraction, emphasizing the advancements and challenges encountered. It also discusses chemical extraction methods applied across different feedstock and microbial strains, highlighting their role in enhancing efficiency and sustainability. This comprehensive review underscores the imperative for advancing PHA technologies, particularly in refining extraction techniques, to facilitate broader adoption in industries seeking environmentally friendly alternatives to conventional plastics. [ABSTRACT FROM AUTHOR]