Plastic Waste Research Articles

Negotiating Plastics: De-mythicizing Individual Responsibility and Plastic Materialities in Japan, from the 1940s to the 1970s

ABSTRACT Japan is the second-largest producer of plastic waste. The government has implemented policies that encourage individual citizens to recycle and reduce plastic products to promote sustainability. This study into the history of women’s relationship with plastics de-naturalises two assumptions embedded in such environmental policies: firstly, the idea that it is the responsibility of individuals to combat the proliferation of plastics and pollution, and secondly, the notion of ‘plastics’ as a singular element to be accepted or rejected. Based on archival research of articles published in the Asahi shimbun and women’s magazines from the 1940s to the 1970s, this article chronicles changing themes in the depiction of women – plastics relationships. The history of women that emerged from the analysis shows that during this period women exercised their power collectively to negotiate the introduction of various plastic elements into the household. Women collectively determined what could be sold as a plastic product, changed the industry and shop floor practices, and influenced law and government policies regarding plastic waste disposal. The analysis reveals that such collective activities played a role in shaping a diverse history of plastics that is often lost in contemporary discourses of a single ‘plastic’ element and individual responsibility.

Recovery of Bis(2-hydroxyethyl) terephthalate and terephthalic acid from waste PET bottles for synthesis of cerium-based metal-organic frameworks: A study towards supercapacitor applications

Controlled chemical recycling of plastic waste is a most important concern to reduce plastic waste as well as effective recovery of the various byproducts without toxic emission. In this study, we focused on effective recovery of Bis-2-hydroxyethylene terephthalate (r-BHET) from polyethylene terephthalate (PET) waste via solvent free melt depolymerization process. Recovered BHET was converted into terephthalic acid (r-TPA) by hydrolysis. Both r-BHET and r-TPA were used to construct a metal organic framework (MOF) with cerium metal for potential energy applications. Extensive characterization, including Fourier Transform Infrared Spectroscopy (FTIR), Nuclear Magnetic Resonance (NMR), Field Emission Scanning Electron Microscopy (FE-SEM), and Energy-Dispersive X-ray Spectroscopy (EDX) were confirmed the structural integrity and purity of the r-BHET and r-TPA and provides insights into the well-defined structure and elemental composition of the MOFs. The specific capacitances of BHET and TPA-Ce-MOF were found to be 91.5 and 220.1 F/g respectively. Comprehensive characterization ensures the quality of the recovered products and synthesized MOFs, promoting environmentally conscious strategies in materials synthesis and energy storage applications.

Microbial consortia for multi-plastic waste biodegradation: selection and validation

The accumulation of plastic waste in the environment poses significant ecological and health risks. This study evaluates the effectiveness of microbial consortia in degrading various types of plastics, including low-density polyethylene (LDPE), low linear-density polyethylene (LLDPE), polyethylene terephthalate (PET) and polystyrene (PS). Qualitative enzyme assays for esterases and ligninases, which are related to plastic biodegradation, were conducted in five microbial strains. Four microbial consortia, combining bacterial and fungal strains, were assembled based on the enzyme profile of their components and evaluated for their ability to degrade both virgin and recycled plastics. The results showed that consortia C2 (Bacillus subtilis RBM2, Fusarium oxysporum RHM1, and Alternaria alternata RHM4) and C4 (Bacillus subtilis RBM2 and Pseudomonas alloputida REBP7) exhibited the highest biodegradation efficiency, particularly achieving significant weight loss in recycled LDPE, virgin LLDPE and recycled PET. The biodegradation was further confirmed by FTIR analysis, which revealed changes in the chemical composition and functional groups of the treated plastics, indicating microbial interaction and degradation. This study underscores the potential of microbial consortia in addressing plastic pollution, highlighting the importance of strategic consortia design based on enzymatic profiles and plastic colonization capabilities. These promising results suggest that further optimization of microbial consortia could offer a viable solution for large-scale plastic waste management.

Polymer Nanocomposites: A Review on Recent Advances in the Field of Green Polymer Nanocomposites

Abstract: In order to address environmental issues, polymer nanocomposites are becoming more and more popular because of their remarkable functionality. Their use in various fields is highlighted by their special physicochemical features (i.e., stability, high reactivity, robustness, regenerability, etc.), conductivity, electronic compatibility, quick interfacial contacts, simplicity of functionalization, simplicity of synthesis, interface-to-volume ratio, and low cost. Green polymer nanocomposites have drawn a lot of attention for use in a variety of applications to preserve the environment. Because they are made of eco-friendly materials, they are frequently utilised in the automobile, building, packaging, and medical industries. Eco-friendly solutions to the problems caused by plastic trash are biodegradable polymers produced from renewable sources (microbes, plants, and animals). Plant fibres and natural resins are combined to create green composite materials. These fibres and resins used in green composites can be broken down by bacteria. The mixing of natural fillers and organic polymers results in green polymer nanocomposites with distinct characteristics. This review is anticipated to be comprehensive, compelling, and practical for the scientists and business professionals who collaborate to address a variety of environmental problems on a global scale using green polymer nanocomposites.

Simulation of Pyrolysis Process for Waste Plastics Using Aspen Plus: Performance and Emission Analysis of PPO-Diesel and PPO-Biodiesel Blends

As the global population increases, so does the usage of plastics in households, water bottles, and garbage bags, posing significant environmental threats. Plastics, being inorganic waste with long degradation periods, contaminate air, water, and soil when disposed of in landfills. Given the rise in global plastic production, effective waste management strategies are essential. This study utilized Aspen Plus simulation to analyze the pyrolysis process of waste plastics, specifically PE, PS, and LDPE. Simulations were conducted with temperature variations between 350°C to 550°C to determine the optimum conditions. Additionally, the study compared engine performance and emissions using mixtures of plastic pyrolysis oil (PPO), biodiesel from waste cooking oil (WCO), and diesel. Engine performance tests were conducted with variations in engine speed and load for PPO-diesel and PPO-biodiesel mixtures. Simulation results showed that the optimal pyrolysis temperature for the highest PPO yield was 450°C, producing 89% for PS plastic. Pyrolysis at 500°C yielded 85% oil for PE, 83% for LDPE, and 60% for mixed plastics. Engine performance tests indicated that adding PPO to diesel and WCO biodiesel significantly affected engine performance and emissions. A 5% PPO blend in diesel demonstrated better brake thermal efficiency and lower BSFC compared to higher PPO blends.

Study on the effects of aging on the pyrolysis of plastic and the synergistic mechanisms of co-pyrolysis with lignite

Co-pyrolysis of waste plastic with low-rank coal explored how photoaging impacts the pyrolysis of plastics and delves into the synergistic mechanisms involved in co-pyrolysis. The results of elemental analysis, X-ray powder diffraction and Fourier transform infrared spectroscopy showed that photoaging primarily involves oxidizing and breaking the aliphatic chains in polyethylene (PE), as well as generating oxygen-containing functional groups like hydroxyl (-OH), carbonyl (-C=O), and ether (-C-O), thereby reducing the crystallinity of PE. The results of individual plastic pyrolysis showed that photoaging is beneficial to the generation of gas and tar. Pyrolysis tar of PE samples contains significant amounts of alcohols, and olefins and alkynes (O&As). The results of co-pyrolysis indicated that photoaging can enhance the yields of gas and oil from the co-pyrolysis between PE and Naomaohu (NMH) coal. Co-pyrolysis effectively reduced the relative content of O&As in the tar from the pyrolysis of PE samples alone by 8.0%-29.0%. The synergistic mechanism of co-pyrolysis between aged PE and NMH involved supplying a significant quantity of hydrogen and hydroxyl radicals by NMH, which react with alkyl radicals generated from PE pyrolysis, leading to the production of additional alkanes and alcohols. These findings offered new insights for a deeper understanding of the co-pyrolysis behaviors between waste plastic and lignite.

Durability and hardened characteristics of cement mortar incorporating waste plastic and Polypropylene exposed to MgSO4 attack

Annual waste plastic disposal has grown, harming nature. Utilising this waste in concrete production may help preserve building resources. This study tested cement mortar with polyvinyl chloride (PVC) and polypropylene (PP) substituted for sand aggregate at 0, 5, 10, 15, and 20%. The samples were nevertheless exposed to a 10% and 20% MgSO4 solution for a month. The properties of both fresh and hardened materials under these circumstances have been evaluated and contrasted with those evaluated under typical circumstances. For mixes including PP and PVC, the flow diameter increased. The rounded plastic particles provided fewer contact surfaces and less friction among mixtures, which reduced water consumption and improved workability, leading to an increase in slump flow. As the amount of plastic aggregate increases, the compressive strength decreased. Moreover, this pattern might be explained by the weakening of the bond between the surfaces of the plastic aggregate and cement paste. The hydration of cement may also be hampered by the hydrophobic properties of plastic aggregate. Like compressive strength, the splitting tensile strength decreased as the replacement level of plastic ratio increased regardless of its type under all conditions (normal and exposing to MgSO4). PP and PVC fine aggregate in mortar increases sorptivity under all situations. Following screening, those circumstances and PVC have the most impact on compressive strength. increasing PVC and PP at 10% for each of them leads to lower values of compressive and tensile strength. An optimization process was implemented to determine the optimum value of PVC, PP, and MgSO4. It shows that using PVC of 3.9%, PP of 10.1%, and MgSO4 of 19.59% leads to maximum compressive and tensile strength with the minimum cost and CO2 emissions.

Riverbank plastic distributions and how to sample them

As plastic pollution exists in aquatic ecosystems globally, monitoring its abundance and distribution has become crucial for understanding transport pathways, sources, sinks, and impacts. Riverbanks are accumulation zones for plastic, but the selection of monitoring methods is constrained by research goals, available resources, and site-specific conditions. This diversity in approaches has led to disparate datasets, highlighting the need for standardized monitoring protocols. Here, we study the spatial distribution of plastic at the riverbank scale, quantify the uncertainty of existing riverbank methods, and provide recommendations for improved monitoring based on the balance between uncertainty loss and increase in effort. We measured riverbank plastic abundance at eight Dutch riverbanks, categorizing the items using 108 item categories (River-OSPAR). For every riverbank, an area of 100 by 25 meters was subdivided into five-by-five-meter squares, resulting in 100 individual monitored sub-areas. We found riverbank plastic exhibited high spatial variability, with deposition patterns ranging from parallel to the waterline to clustered, random, or uniform (Moran’s I between -0.050 and 0.301). Individual measurements from diverse sampling protocols are 5-49 times less accurate than estimates derived from extensive sampling, highlighting the diminishing impact of specific methods with increased data collection. Lastly, our findings suggest that increasing the sampling area quickly reaches diminishing returns in terms of accuracy. Reducing the sampled area by 80% only increases the uncertainty in estimating the true plastic density by 20%. While standardized protocols are essential for data comparability, a rigid, uniform sampling approach may be less efficient and resource-intensive than a flexible (step-wise) strategy that adapts to local conditions. By demonstrating that extensive sampling can mitigate the differences between unique sampling protocols, this study promotes a shift towards flexible and efficient riverbank plastic monitoring, ultimately accelerating global efforts to combat plastic pollution.

Toxicological effects and potential reproductive risk of microplastic-induced molecular changes in protamine-like proteins and their DNA binding

Today, plastic pollution is a widespread problem in all ecosystems and has a particularly severe impact on marine ecosystems and external fertilisers such as the mussel Mytilus galloprovincialis. The present study aims to assess the toxicological reproductive health effects in this organism following exposure to two concentrations of polystyrene microplastics (PS-MPs) (0.5 and 1 μg/L), representative of conditions in the Mediterranean Sea. After exposure, the electrophoretic pattern of protamine-like (PL) proteins, the major basic protein component of Mytilus galloprovincialis sperm chromatin, was analysed. Compared to the unexposed condition, differences were observed by SDS-PAGE and an increased ability of PL to bind and protect DNA from oxidative damage was then measured, particularly for PL from mussels exposed to 1 μg/L PS-MPs. At this dose of PS-MPs, a reduced release of all PLs from the sperm nuclei was also observed, whereas the digestion by micrococcal nuclease did not show any significant differences between the exposed and the unexposed conditions. Finally, the possibility of poly(ADP)-ribosylation of the PLs was investigated. PL-II showed an increase in poly(ADP)-ribosylation after PS-MPs exposure, which may account for the difference in the ability of the PLs to bind DNA. In conclusion, while all the results might suggest a molecular mechanism of gametic plasticity occurring upon exposure of mussels to PS-MPs 1 μg/L, they also indicate that this dose of exposure could be extremely detrimental to the reproductive health of Mytilus galloprovincialis because it could prevent the release of basic nuclear proteins from the sperm DNA at fertilisation.

Trophic transfer effects of PS nanoplastics and field-derived nanoplastics in the freshwater clam Corbicula fluminea

Plastic pollution is of global concern. Many studies investigated the effect of micro and nanoplatics towards aquatic organisms. However, relatively few studies were assessed on freshwater organisms. Another aspect of this pollution is the impact of trophic transfer on plastic distribution and on food chain in order to evaluate its potential risk towards environmental and human health. In this context, the objective of this study was to assess the ecotoxicological impacts of different types of nanoplastics (NPs) on freshwater organisms exposed through trophic transfer. Freshwater microalgae Scenedesmus subspicatus were contaminated for 48 hours with realistic concentrations of NPs (0.008, 10 and 100 µg/L). Two types of NPs were tested: commercial PS NPs and NPs generated from macro-sized plastics collected in the field (ENV NPs). Freshwater Corbicula fluminea bivalves were then fed with the contaminated algae every 48h for 21 days. Results showed that trophic exposure led to the induction of oxidative stress (CAT activity). Overall, NPs trophic exposure caused downregulations of genes implicated in many cellular processes (immunity, oxidative stress, neurotoxicity, endocytosis, apoptosis).This present study allowed to demonstrate the relevance of investigating the trophic transfer effects of NPs on a freshwater trophic chain. Further studies should focus more on larger levels of the food chain.

Evaluating microplastic particles as vectors of exposure for plastic additive chemicals using a food web model

Microplastic particles (MPs) represent potential hazards for humans and wildlife, including as vectors for chemical exposure (e.g. plastic additives and pollutants sorbed from the surrounding environment). The leaching of chemicals from MPs has been identified as a potential exposure pathway but the relative magnitude of this pathway under environmentally relevant conditions remains unclear. Here, we describe a modification of the ACC-HUMANSTEADY bioaccumulation model to include dietary exposure to MPs containing either accumulated chemicals from the surrounding environment or embedded plastic additive chemicals (PACs). Chemical transfer to humans and wildlife is described using two-film resistance concepts assuming spheroidal particles of different sizes. The relative contribution of MPs and environmental media to the estimated daily chemical intake in humans was assessed in various exposure scenarios, for a range of hypothetical chemicals with varying octanol-water and air-water partition coefficients (KOW and KAW, respectively; i.e. 0 < log KOW <8 and − 5 < log KAW < 3). Results imply that MPs could act as sources of exposure to chemical additives when the ingestion rate of 1 μm MPs is ≥ 10 mg d− 1, and the concentration of hydrophobic plastic additive is ≥ 5% wt wt− 1. The contribution made by MPs as vectors of exposure decreased with increasing particle size and decreasing ingestion rates of MPs. Human health risks were evaluated for four specific PACs to illustrate the application of the model for risk assessment. Risks were negligible when the ingestion rate of MPs was < 100 μg d− 1. Uncertainties are high regarding the characterization and quantification of ingestion of MPs by humans and wildlife, including particle sizes and polymer composition, as well as on the presence of PACs in MPs. These data gaps need to be addressed if the issue of MPs as vectors of chemical exposure is to be fully understood. The work illustrates that mechanistic models, which account for all major exposure pathways, can be used to identify the importance of different exposure pathways, help prioritize research needs and support decision making.

Biopolymers for a Sustainable Food System: Sources, Applications, and Environmental Impacts

ABSTRACTThe use of synthetic polymers in the food industry poses significant risk of contamination, global plastic waste, and pollution. In contrast, biopolymers offer a potential solution for a sustainable future. Derived from natural resources, biopolymers are biodegradable and compostable and do not leach hazardous chemicals into food, which make them ideal for various applications in the food industry, owing to the non‐leaching of hazardous chemicals into the food. Here, an overview of the potential of biopolymers to replace synthetic plastic in food is discussed. The degradation of biopolymers and their environmental impact, the formation of biopolymer films, the utilization of different biopolymers for sustainable solutions to synthetic polymers, and their advantages are thoroughly presented. This review is expected to guide food industry stakeholders in seeking biopolymers as sustainable and eco‐friendly alternatives to synthetic polymers.

Biodegradation of commercial polyester polyurethane by a soil-borne bacterium Bacillus velezensis MB01B: Efficiency, degradation pathway, and in-situ remediation in landfill soil

Polyurethane (PU), a widely used and durable plastic, persists in the environment, resulting in significant waste management challenges. Therefore, developing eco-friendly degradation technologies, such as screening for efficient biodegrading microorganism strains, is urgently needed to address this issue. Bacillus velezensis MB01B, an efficient polyester PU-degrading bacterium, was isolated from landfill soil and demonstrated the ability to degrade 91.4% of 0.75% Impranil DLN within 24 h under the optimal conditions (30.5 °C and initial pH 6.5). To assess the degradation capability of MB01B, three PU substrates of increasing complexity—Impranil DLN film, polyester thermoplastic polyurethane (TPU) film, and commercial PU desk mat—were tested; after 30 days, weight losses of 24.8%, 18.3%, and 5.4% were observed, respectively. In addition, SEM images showed significant morphological changes on the surface of these PU materials after treatment with MB01B. FTIR analysis of Impranil DLN films following degradation showed reductions in key functional groups (ester and urethane); and the identification of neopentyl glycol and 1,6-hexanediol as degradation intermediates suggested MB01B possesses the capability to hydrolyze ester and urethane bonds. Concurrently, genome sequencing combined with RT-qPCR identified several enzymes, including urethanases and esterases/lipases, involved in PU degradation. Based on these results, the pathway for MB01B to degrade Impranil DLN was inferred. Finally, MB01B was successfully formulated into a solid microbial inoculum with favorable storage properties and used for in-situ degradation of the commercial PU materials (Impranil DLN films, TPU films and PU desk mat) in landfill soil, underscoring its potential for the in-situ biological treatment of PU plastic wastes.

Boosting light olefin production from pyrolysis of low-density polyethylene: A two-stage catalytic process

The increasing production of waste plastics poses significant environmental and health risks. Low-density polyethylene (LDPE), a major component of plastic waste, is a high-quality feedstock for pyrolysis due to its high carbon and hydrogen content. Traditional pyrolysis methods, such as thermal cracking and one-step catalytic pyrolysis, have limitations in yield and selectivity of valuable products like light olefins. This study introduces a two-stage catalytic pyrolysis (TSCP) process aimed at enhancing the production of light olefins from LDPE. In the first stage, LDPE undergoes pyrolysis with MCM-41 catalyst, yielding a substantial number of liquid products and a minor portion of light olefins. The second stage utilizes Mg-ZSM-5 catalyst to further crack the high-temperature volatile matter into light olefins. The optimal conditions identified were 450 °C in the first stage and 500 °C in the second stage, achieving a maximum light olefin yield of 45.80 wt% and a low reaction temperature, decreasing the energy consumption. Additionally, the MCM-41 catalyst demonstrates excellent regeneration performance, with only a slight decrease in liquid yield after nine cycles. The Mg-ZSM-5 catalyst maintains high stability, with light olefin yield remaining at 83.60 % of the initial yield after 48 h of operation.

Combined thermochemical-biotechnological approach for the valorization of polyolefins into polyhydroxyalkanoates: Development of an integrated bioconversion process by microbial consortia

Waste management of persistent polymers such as polyolefins (PO)1 still represents a major challenge, often leading to material loss from the value chain and contributing to plastic pollution. This study investigated an integrated process to valorize PO pyrolysis side stream. PO wax was recovered and used as a feedstock for a microbial bioconversion process. A modified emulsification protocol (using two-surfactants system) allowed the successful dispersion and bioconversion of PO wax without the need of the extra oxidation step. Enrichment of plastic landfill inocula allowed to develop efficient mixed microbial consortia (MMC) able to grow on PO wax. Adaptive laboratory evolution improved 4 times cell growth, leading to 2.6–17.3 times shorter lag phase. The bioconversion process using the adapted MMC was performed in a 2 L-bioreactor with PO wax-emulsified media (10 g L−1) at neutral pH and 20% pO2. 87% of substrate was consumed within 12 h and complete consumption was achieved within 48 h (4 times faster than previously reported). A maximum of 2.95 gCDW L−1of biomass was produced, while the intracellular triglycerides reached a maximum of 105.5 mg L−1 at 30 h. Moreover, the conversion of PO wax into polyhydroxyalkanoates (PHAs) was demonstrated and the production was maximized by statistical optimization. Maximum PHA titer of 384 0.1 mg L−1 was achieved, which represents a 1.5–17 times improvement from previous reports. This integrated thermochemical-biotechnological approach might represent an interesting strategy to valorize and upcycle currently unrecyclable PO-rich mixed plastic waste streams, thus improving the circularity of the plastic sector.

Cutting‐Edge Strategies and Advancements for Combating Synthetic Polymer Pollution in Various Environmental Samples: A Review

AbstractPlastic debris is unavoidably released into the ecosystems, and their physicochemical and mechanical qualities deteriorate when exposed to the environment. This, ultimately, leads to the generation of tiny fragments of plastic, which are known as nanoplastics (&lt;1000 nm) and microplastics (&lt;5 mm). Over the past few years, the pollution of synthetic polymers has been reported in almost all the compartments of the environment across the globe. It is regarded as a hazard to both human health and natural systems. In addition, synthetic polymers act as vectors for contaminants as they can adsorb and accumulate contaminants from seawater. The accumulation of plastic waste in the environment and its widespread presence have drawn the attention of policymakers and the public. This global issue has led to the creation of numerous remediation solutions by innovators in previous decades, either to clear up old waste or to stop plastic from entering the various matrices of the environment. This review focused on the extensive scientific research available on effective techniques for removing plastic debris to promote positive action and progress in this important area. Despite the various challenges, these techniques offer vital opportunities, from increasing awareness to enhancing environmental quality. Further, the article has been enriched by incorporating bibliometric data that illustrates the widely used methods for removing microplastics from various environmental matrices. According to the data analysis, numerous remediation techniques have been developed to date (2010 and 2024). These techniques encompass various approaches, among which the chemical‐based methods enjoy more success. This success can be attributed to the diverse advantages offered by chemical‐based methods over other remediation techniques. Much research is now focused on overcoming the disadvantages and developing more efficient and environmentally sound technologies.

Uranium and arsenic bioremediation potential of plastic associated multi-metal tolerant Bacillus sp. EIKU23

Plastic waste accumulation is a significant environmental concern as it promotes microbial growth and acts as a carrier for heavy metals. This study focuses on a Bacillus sp. strain isolated from the surface of a used plastic bottle, tolerant to various potential toxic elements (PTEs) such as chromium, nickel, cobalt, copper, zinc, arsenite [As(III)], but sensitive to uranium (U) and arsenate [As(V)] toxicity. The strain demonstrates growth under different abiotic stress conditions, with the optimal pH range of 5.0-8.0 and a temperature of 30 °C. It shows remarkable removal capabilities, removing >23.3% of U, >38% of As(III)), and >22.6% of As(V) from an initial dose of 100mgL−1 in an aqueous solution. The biosorption capacity for U, As(III), and As(V) is 3.12, 3.1, and 1.8mgg−1 of biomass, respectively. Kinetic modelling suggests that the biosorption of U and As(V) follows a pseudo-second-order mechanism, while As(III) biosorption follows a pseudo-first-order mechanism. Moreover, the strain has the ability to precipitate >38.1% and ~67% of U using bacterially released phosphate from inorganic and organic sources, respectively. These findings highlight the strain's potential for bioremediation of PTE-contaminated environments, providing valuable insights for optimizing metal removal and immobilization processes in future research.

Assessing Environmental Impacts of Various Solvent-Dissolution Routes for the Pelletization of Mixed Plastic Waste

Assessing Environmental Impacts of Various Solvent-Dissolution Routes for the Pelletization of Mixed Plastic Waste

Effects of acid and sulphate attack on concrete containing recycled plastic waste fine aggregate

Effects of acid and sulphate attack on concrete containing recycled plastic waste fine aggregate

Superhydrophobic poly(lactic acid) membrane prepared with the induction of modified carbon dots for efficient separation of water-in-oil emulsions

Superhydrophobic separation membranes are considered to be one of the most promising technologies for oil-water separation. However, the plastic waste generated from discarded membranes poses a challenge to the preparation of degraded superhydrophobic separation membranes for achieving eco-friendly separation. In this study, superhydrophobic poly(lactic acid) (PLA) membranes were fabricated using a non-solvent induced phase separation method assisted by l-cysteine modified carbon dots (Cys-CDs). The synergistic effect of Cys-CDs-induced crystallization behavior of PLA and the phase separation process results in the evolution of the surface of the PLA-based membrane from a pistil-like structure to a multi-level micro-nano structure composed of dense lamellar nanofibers and microspheres with an increase in Cys-CDs content. At a Cys-CDs content of 5 wt%, the surface roughness of PLA-based separation membrane reached its maximum, and the water contact angle was as high as 159°. Remarkably, the superhydrophobic Cys-CDs/PLA membrane exhibited promising performance in the separation of water-in-oil emulsions, with a rejection rate of 99.98 % and a flux of 315.74 L·m−2·h−1·bar−1. Additionally, the superhydrophobic Cys-CDs/PLA separation membrane also demonstrates impressive properties such as acid-alkali resistance and rapid recycling into high-value chemicals. Consequently, this rapidly recoverable superhydrophobic porous Cys-CDs/PLA membrane shows great potential for practical applications in actual oil-water separation.