Can on-site leachate treatment facilities effectively address the issue of perfluoroalkyl acids (PFAAs) in leachate?

In recent decades, the presence of perfluoroalkyl acids (PFAAs) in municipal solid waste leachate has emerged as a growing concern. Research has focused on PFAA release and occurrence characteristics in landfill and waste-to-energy leachate, highlighting their significant impact when released into wastewater treatment plants. Given the extremely high loading rate faced by current on-site leachate treatment plants (LTPs), the objective of this study is to assess whether the current "anaerobic/aerobic (A/O) + membrane bioreactor (MBR) + nanofiltration (NF) + reverse osmosis (RO)" configuration is effective in PFAAs removal. Concentrations of raw and treated leachate in 10 on-site LTPs with same treatment configuration and varying landfill ages were measured, and a comprehensive mass flow analysis of each treatment process was conducted. The results indicate that A/O treatment has limited capacity for PFAA removal, while NF and RO processes reached 77.44 % and 94.30 % removal rates of ∑PFAAs concentration, respectively. Short-chain PFAAs (> 80 % detected frequency) primarily influenced the distribution and variations of PFAAs in leachate and tend to disperse in the water phase. Correlation analysis revealed the current on-site LTPs exhibit a more efficient removal capacity for long-chain PFAAs.

Separation of Chloride and Sulfate Ions from Desulfurization Wastewater Using Monovalent Anions Selective Electrodialysis.

The high concentration of chloride ions in desulphurization wastewater is the primary limiting factor for its reusability. Monovalent anion selective electrodialysis (S-ED) enables the selective removal of chloride ions, thereby facilitating the reuse of desulfurization wastewater. In this study, different concentrations of NaCl and Na2SO4 were used to simulate different softened desulfurization wastewater. The effects of current density and NaCl and Na2SO4 concentration on ion flux, permselectivity (PSO42-Cl-) and specific energy consumption were studied. The results show that Selemion ASA membrane exhibits excellent permselectivity for Cl- and SO42-, with a significantly lower flux observed for SO42- compared to Cl-. Current density exerts a significant influence on ion flux; as the current density increases, the flux of SO42- also increases but at a lower rate than that of Cl-, resulting in an increase in permselectivity. When the current density reaches 25 mA/cm2, the permselectivity reaches a maximum of 50.4. The increase in NaCl concentration leads to a decrease in the SO42- flux; however, the permselectivity is reduced due to the elevated Cl-/SO42- ratio. The SO42- flux increases with the increase in Na2SO4 concentration, while the permselectivity increases with the decrease in Cl-/SO42- ratio.

Four-decades evolutionary development of municipal solid waste management in China: Implications for sustainable waste management and circular economy.

This study collected data on waste generation and management in China between 1979 and 2020 from government statistics and literature and reviewed the development of municipal solid waste (MSW) management in China. The extended stochastic impact by regression on population, affluence and technology (STIRPAT) model was employed to identify the driving forces of MSW generation, and the cointegration analysis showed that economy (0.35, t = -3.47), industrial structure (3.34, t = -20.77) and urbanization (-1.5, t = 5.678) were the significant socioeconomic driving forces in the long run. By employing the framework of evolutionary economics, this study then investigated the internal rules of long-term interaction between socioeconomic factors and MSW management. The results indicate that, in the long run, MSW management development can be viewed as an evolutionary process that includes a continuous adaptation to external socioeconomic factors and the co-evolution of internal institutions and technologies. Adaptation and diversity of institutions and technologies play an important role in achieving sustainable waste management and circular economy (CE). This study offers a novel evolutionary perspective for explaining dynamic changes of MSW management in China, as well as recommendations for emerging economies to achieve sustainable waste management and CE goals.

Superhydrophobic Nanoparticles: An Efficiently Selective Adsorbent for Surfactant-Like Contaminants from Complex Wastewater Matrices.

Surfactant-like contaminants (SLCs) with distinctive amphiphilic structures have become a global concern in wastewater due to their toxicity and persistency. Despite extensive efforts, achieving efficient and selective SLCs removal remains challenging because of their wide range of molecular weights and complex functional group compositions. Superhydrophobic nanoparticles can potentially tackle this challenge by targeting the long oleophilic chains of SLCs. However, conventional contact angle measurements hinder hydrophobicity characterization and corresponding selectivity research because of the powder morphology of nanoparticles. Herein, the authors offered information regarding the distribution of water molecular probes in surfaces and proposed a quantitative characterization approach based on low-field nuclear magnetic resonance. Through synthesizing superhydrophobic and hydrophilic polydopamine nanospheres with similar morphologies, the selective adsorption potential of superhydrophobic nanoparticles for SLCs is systematically demonstrated. As revealed by the interaction mechanisms, the superhydrophobic surface of nanospheres increased its affinity and selectivity for SLCs adsorption by enhancing hydrophobic interactions. Superhydrophobic modification achieved ten times the adsorption capacity of sodium dodecyl benzene sulfonate, an exemplified surfactant, compared with pristine nanoparticles. By regulated self-polymerization, the superhydrophobic nanospheres are coated onto the surface of a 3D sponge and enable efficient selective SLCs adsorption from highly polluted leachate matrices with long-term stability and reusability.

The Adsorption Behaviors and Mechanisms of Humic Substances by Thermally Oxidized Graphitic Carbon Nitride.

Thermal oxidation is efficient for enhancing the photocatalysis performance of graphitic carbon nitride (g-C3N4), while its effect on adsorption performance has not been fully studied, which is crucial to the application of g-C3N4 as adsorbents and photocatalysts. In this study, thermal oxidation was used to prepare sheet-like g-C3N4 (TCN), and its application for adsorption of humic acids (HA) and fulvic acids (FA) was evaluated. The results showed that thermal oxidation clearly affected the properties of TCN. After thermal oxidation, the adsorption performance of TCN was enhanced significantly, and the adsorption amount of HA increased from 63.23 (the bulk g-C3N4) to 145.35 mg/g [TCN prepared at 600 °C (TCN-600)]. Based on fitting results using the Sips model, the maximum adsorption amounts of TCN-600 for HA and FA were 327.88 and 213.58 mg/g, respectively. The adsorption for HA and FA was markedly affected by pH, alkaline, and alkaline earth metals due to electrostatic interactions. The major adsorption mechanisms included electrostatic interactions, π-π interactions, hydrogen bonding, along with a special pH-dependent conformation (for HA). These findings implied that TCN prepared from environmental-friendly thermal oxidation showed promising prospects for humic substances (HSs) adsorption in natural water and wastewater.

Identification of key surfactant in municipal solid waste leachate foaming and its influence mechanism.

Serious foaming problems and the excessive consumption of defoamer have undoubtedly become one of the most critical problems that hinder municipal solid waste (MSW) leachate treatment efficiency and industry development. Since there is limited research penetrating the foaming mechanism and identification of the key surfactants, current defoaming and surfactant removal techniques lack pertinence and orientation. In this study, a foaming characterization device was developed and ultra-performance liquid chromatography-tandem mass spectrometry (UPLC/MS/MS) was optimized to accurately identify the key surfactants affecting leachate foaming and offer a glimpse into their interaction mechanisms. This study collected leachate samples from 9 typical landfills and waste-to-energy facilities of various waste compositions, climatic conditions, ages, and geographical locations. The foaming problem of leachate was mainly centered on raw leachate and nanofiltration membrane concentrate (NFC). Fresh leachate performed with relatively low foaming capacity and foam stability, associated with low surfactant concentration. The pH value of the system was positively correlated with the concentration of anionic surfactants, indicating significant impacts on surfactant release in MSW. Since the distribution characteristics of linear alkylbenzene sulfonate (LAS) in leachate were consistent with the variety of foaming performances, LAS proved to be an indispensable surfactant in the leachate involved in this study, and its content proportion escalated to 92.87% in aged leachate.

Occurrence and removal of per- and polyfluoroalkyl substances (PFAS) in leachates from incineration plants: A full-scale study.

Municipal solid wastes (MSWs) contain diverse per- and polyfluoroalkyl substances (PFAS), and these substances may leach into leachates, resulting in potential threats to the environment and human health. In this study, leachates from incineration plants with on-site treatment systems were measured for 17 PFAS species, including 13 perfluorocarboxylic acids (PFCAs) and 4 perfluorosulfonic acids (PFSAs). PFAS were detected in all of the raw leachates and finished effluents in concentrations ranging from 7228 to 16,565 ng L-1 and 43 to 184 ng L-1, respectively, with a greater contribution from the short-chain PFAS and PFCAs. The results showed that the existing combined processes (biological treatment and membrane filtration) were effective in decreasing PFAS in the aqueous phase with removal efficiencies over 95%. In addition, correlation analysis suggested that physical entrapment, not biodegradation, was the main means of PFAS reduction in the treatment system. These results filled a gap in the understanding of PFAS occurrence and removal in leachates from incineration plants during the full-scale treatment processes, and demonstrated those leachates were previously under-explored sources of PFAS.

Reduction capacity of humic acid and its association with the evolution of redox structures during composting.

The reducing capacity (RC) of compost-derived humic acid (HA) is related to the type and number of redox-active functional moieties in its structure and has a considerable environmental influence on its geochemical redox cycle. Composting treatment can affect the redox-active fractions of organic substances through microbial transformation and degradation. However, the relationship between the RC of compost-derived HA and its fluorescence component and infrared spectra remains unclear. In this study, we assessed the response of the organic reducing capacity (ORC) and inorganic reducing capacity (IRC) of compost-derived HA to the stabilization of organic solid waste materials by analyzing the redox-active functional groups of HA extracted at different composting times. The results demonstrated that the RC of compost-derived HA continuously increased during composting because of the formation of fulvic- and humic-like fluorescent components, which consist of amide, phenolic hydroxyl, quinone, and aromatic groups. Adsorption occurred between HA and FeCit by aliphatic and out-of-plane aromatic CH, which released free hydrogen and increased the Fe-binding site; consequently, ORC was obviously higher than IRC. The results of this study could provide an understanding of the transformation of the fluorescent substances and functional groups that affect redox properties during composting; therefore, this study has considerable significance for exploring the application of compost products.

Treatment of wastewater using black soldier fly larvae, under different degrees of biodegradability and oxidation of organic content.

The biological treatment process based on the metabolism of Black Soldier Fly (BSF) larvae proved to be a highly promising technique for the treatment of high organic content (HOC) wastewater, such as sewage from food industries, leachate from municipal solid waste (MSW) landfill, etc. The present study was aimed at achieving a better understanding of how biodegradability and degree of oxidation of organic content might influence treatment performance and biomass quality. Six leachates characterised by similar COD (Chemical Oxygen Demand) but different BOD5/COD (Biochemical Oxygen demand/COD) and TOC/COD (Total Organic Carbon/COD) ratios were tested. By combining these ratios, the BOD5/TOC ratio was introduced to take into account the effect of both leachate properties (biodegradability and oxidation degree). Process treatment performance was significantly influenced by the quality of organic substances. Higher BOD5/TOC values (higher biodegradability and lower oxidation degree) resulted in a greater and faster larvae growth, with final wet weight of between 49.2 and 91.9mg/larva; lower mortality between 5 and 32%; higher prepupation percentages ranging from 4 to 21% and higher specific substrate consumption rate with values varying from 0.051 to 0.063 mgTOC/mg larva/d, up to 3-fold higher than values obtained using conventional activated sludge based on COD consumption. Conversely, no significant differences were detected in larvae protein and lipid contents, including the profiling of fatty acids.

Occurrence of per- and polyfluoroalkyl substances (PFAS) in municipal solid waste landfill leachates from western China.

Landfill leachate has been documented as a significant source of trace organic pollutants, comprising an expansive family of per- and polyfluoroalkyl substances (PFAS). This study presents the findings on the distribution of 13 perfluoroalkyl carboxylates (PFCAs) and 4 perfluoroalkyl sulfonates (PFSAs) in leachates from 6 municipal solid waste (MSW) landfills in western China. The total concentrations of 17 PFAS in sampled leachates ranged from 1805 to 43,310 ng/L, and 15 compounds were detected in all samples. The short-chain compounds perfluorobutane sulfonate (PFBS, mean mass fraction 23.1%) and perfluorobutyric acid (PFBA, mean mass fraction 20.6%) were dominant. There were higher PFAS concentrations in leachates from operating landfills (mean: 12,194 ng/L) compared to closed landfills (mean: 2747 ng/L), but there was no significant difference between young (< 10 years) and old landfills (> 10 years). Moderate to weak correlations were observed between PFAS concentrations and leachate properties, e.g., TN, NH4+-N, TOC, and pH. This is the first report on the distribution of PFAS in landfill leachates from western China. The results have identified landfill leachate as an underestimated source of PFAS in the environment and have contributed to a more comprehensive evaluation on PFAS presence across China.

Preparation of artificial MSW leachate for treatment studies: Testing on black soldier fly larvae process.

When approaching the study of new processes for leachate treatment, each influencing variable should be kept under control to better comprehend the treatment process. However, leachate quality is difficult to control as it varies dramatically from one landfill to another, and in line with landfill ageing. To overcome this problem, the present study investigated the option of preparing a reliable artificial leachate in terms of quality consistency and representativeness in simulating the composition of real municipal solid waste (MSW) leachate, in view of further investigate the recent treatment process using black soldier fly (BSF) larvae. Two recipes were used to simulate a real leachate (RL): one including chemical ingredients alone (artificial synthetic leachate-SL), and the other including chemicals mixed with artificial food waste (FW) eluate (artificial mixed leachate-ML). Research data were analysed, elaborated and discussed to assess simulation performance according to a series of parameters, such as Analytical representativeness, Treatment representativeness (in this case specific for the BSF larvae process), Recipe relevance, Repeatability and Flexibility in selectively modifying individual quality parameters. The best leachate simulation performance was achieved by the synthetic leachate, with concentration values generally ranging between 97% and 118% of the RL values. When feeding larvae with both RL and SL, similar mortality values and growth performance were observed.

Enhanced adsorption of humic/fulvic acids onto urea-derived graphitic carbon nitride.

Since humic substances (HSs) can cause environmental problems, their elimination has been attracting more and more concerns. In this study, we investigated HSs adsorption onto urea-derived graphitic carbon nitride (CNU) and elucidated adsorption mechanisms (i.e. heterogeneity, interface rearrangement, and multiple interactions). The adsorption capacity of CNUs was enhanced as increasing calcination temperature and time. Among CNUs, CNU-575-3 showed the highest adsorption capacity; the maximum adsorption capacities for humic acid (HA) and fulvic acid (FA) were 164.06 mg C/g, 14.61 L/cm·g, 91.12 mg C/g, and 5.34 L/cm·g, respectively. The adsorption affinity of CNUs mainly correlated with the amount of amino groups, and that of HSs components was dependent on aromaticity due to π-π interactions. More specifically, terrestrial humic-like and fulvic-like components within HA and FA showed the greatest adsorption affinity, respectively. HSs adsorption was remarkably affected by pH, alkali metals, and alkali earth metals via electrostatic interactions, H-bonding, cation bridge, and configurational effect. In addition, the adsorption of Elliott soil HA (ESHA) and the landfill leachate concentrate by CNUs was also highly efficient. This study shows the great promise of CNUs for HSs adsorption in waters and wastewaters.

Life Cycle Assessment of Leachate Treatment Strategies.

Increasingly stringent regulations for leachate discharge call for leachate treatment plants (LTPs) to increase their treatment capacity by adopting membrane treatment processes to remove nitrogen and organics beyond conventional biological treatment processes. This study developed four common treatment strategies based on the existing operation and construction conditions of seven representative LTPs in China. We evaluated the LTPs' environmental impacts using life cycle assessment (LCA) following the International Organization for Standardization (ISO 14040 and ISO 14044). Compared with conventional secondary treatment processes, implementing high-level technologies to meet the strict standards could reduce an average of 59% of the eutrophication potential while increasing other environmental impacts resulting from both direct and indirect emissions by an average of 146%. We propose advanced technologies that integrate both midpoint and endpoint LCA results to meet stringent standards in areas sensitive to eutrophication.

Insights into Adsorption of Humic Substances on Graphitic Carbon Nitride.

Graphitic carbon nitride (CN) has been widely used in environmental pollution remediation. However, the adsorption of organic compounds on CNs, which has practical significance for the environmental application of CNs, is poorly understood. For the first time, this study systematically investigated the adsorption behaviors and mechanisms of humic substances (HSs), i.e., humic acid (HA) and fulvic acid (FA), on CNs derived from four typical precursors. Intriguingly, CN derived from urea (CN-U) showed a great capacity for HS adsorption due to its porous structure and large surface area, with maximum adsorption amounts of 73.24 and 51.62 mgC/g for HA and FA, respectively. The formation, influencing factors, and relative contributions of multiple interactions to HS adsorption on CNs were thoroughly elucidated. HS adsorption on CNs was mainly mediated by electrostatic interactions, π-π interactions, and H-bonding. The dominance of electrostatic interactions resulted in HS adsorption being highly dependent on pH and ionic strength. HS components with high aromaticity and high molecular weight were preferentially adsorbed due to π-π interactions. These multiple interactions were largely affected by amino groups and tri-s-triazine units of CNs, as well as the moieties of aromatic rings and oxygen-containing groups of HSs.

Calcium leaching characteristics in landfill leachate collection systems from bottom ash of municipal solid waste incineration.

Calcium leaching is a critical factor in the clogging of leachate collection systems (LCS), a phenomenon that affects landfill stability and operation. The bottom ash (BA) of municipal solid waste (MSW) incineration plants contains large quantities of calcium-based compounds. Landfilling is the main disposal method for BA in China that intensifies the consequences of LCS clogging. The factors influencing BA calcium leaching were investigated using simulated leachate. The results showed that fine BA particles, low pH values, high temperature, and ratios of leachate to BA solids were conducive to calcium leaching. Calcium leaching was found to be higher in actual leachate than in simulated leachate. At pH = 5, the cumulative calcium dissolution ratios (CDRs) were 83.36% and 31.49% after 20 days of leaching in the actual and simulated leachate, respectively; at pH = 6, the values were 50.67% and 12.06%, respectively. The introduction of landfill gas could decrease the calcium dissolution and leaching rates. When the ratio of leachate to BA solid was 20:1 mL/g, the accumulative CDR values were 45.98% (pH = 6) and 5.80% (pH = 8) without landfill gases, and 4.59% (pH = 6) and 0.48% (pH = 8) with landfill gases. These results provide the scientific basis for clogging risk prediction with respect to calcium leaching in the LCS of landfills. BA landfilling in old landfill areas with relatively high leachate pH and low chemical oxygen demand, as well as when leachate mixed with an appropriate amount of landfill gases, could be feasible measures to reduce calcium leaching and further prevent clogging in LCS.

Enhanced darkening effect from the interaction of MnO2 and oxygen on the component evolution of amino-phenolic humic-like substances.

Humification is greatly enhanced by metallic oxides in nature, and the related products are critical to various environmental processes. However, little is known about the interaction between metallic oxides and oxygen in promoting the oxidative polymerization of small organic molecules during the humification process. The synthesis of humic-like acids (HLAs) with MnO2 was performed in the presence and absence of oxygen, and the influence of oxygen and MnO2 on the composition evolution of amino-phenolic HLAs was illustrated. The results of ultraviolet-visible (UV-Vis) spectra of reaction mixtures associated with two-dimensional correlation spectroscopy (2D-COS) combined with the XPS spectra of N 1s content changes in HLAs demonstrated that MnO2 induced pyrrole-type nitrogen formation and enhanced darkening. Furthermore, MnO2 mainly acted as a catalyst, and oxygen activated the regeneration of MnO2 by oxidizing free manganese ions, thus substantially promoting the formation and accumulation of HLAs, whereas it decreased the reaction rate of HLAs formation. Moreover, carbon dioxide release was found during the process of the formation of fulvic-like acids (FLAs), and the reaction was oxygen-independent. Additionally, the formation and transformation of products without MnO2 do not obey kinetics equations, whereas the darkening reaction with MnO2 followed the pseudo-second-order and pseudo-zero-order kinetics equations. These findings provide new insights into the behaviours and fate of the oxygen-mediated humification process and related reaction products.

Effect of submerged combustion evaporation on Cd complexation potential of organic matter in municipal solid waste landfill leachate.

Despite the strong ability for complexation of heavy metals, a high amount of humic substances (HS) is always contained in membrane retentate from municipal solid waste landfill leachates treatment processes. Submerged Combustion Evaporation (SCE) can be used to effectively concentrate the membrane retentate. However, the impact of the SCE treatment on HS complexation capacity is still unclear. Since cadmium (Cd) plays a vital role in the pollution of soil and food, this study investigated the influence of the SCE treatment on the Cd complexation potential of leachate HS. Specific effects and complexation properties on Cd complexation of leachate HS before and after the SCE treatment were demonstrated using the Non-Ideal Competitive Adsorption model. The results showed that the Cd complexation capacity of carboxyl sites increased from 3.76 to 4.65 mol/kg-Total Organic Carbon (TOC) after the SCE treatment, which agreed with the stoichiometric number of proton binding sites. Moreover, characterization results indicated that SCE increased the affinity of HS for Cd by enhancing the overall aromaticity of HS (E2:E4 from 9.8 to 9.3), dominantly due to the humic acid contribution. By modeling the practical Cd remediation scenarios, the enhanced Cd complexation performance of HS after SCE treatment was observed even at low pH values (pH = 5) or insufficient TOC content (TOC = 50 mg/L).

Population dynamics of microbial species under high and low ammonia nitrogen in the alternate layer bioreactor landfill (ALBL) approach.

Anaerobic landfill process is still believed to be a complex ecosystem due to the lack of knowledge on the functional activities of microbial species. This research sought to introduce a novel landfill bioreactor, named here as the alternate layer bioreactor landfill (ALBL) of fresh MSW (FW) and stabilized waste (CT) to avoid inhibitory conditions for the microbial species in anaerobic landfill. The stabilized waste layer in the bottom of landfill cell significantly changed microbial ecology of fresh MSW which in turn reduced the concentrations of NH4-N (29-31%) and VFAs (33-38%) in the ALBL approach, compared to fresh MSW disposal in sanitary landfill. The reduction of NH4-N favored early onset of methanogenesis within 6 weeks and methane (CH4) content of landfill gas increased from 11% to 40-50% (v/v), owing to the coexistence of Methanosarcinales (36-50%) and Methanomicrobiales (26-28%) archaea. The acetoclastic methanogenesis was achieved by reducing NH4-N toxicity in the ALBL.

Insights into Mechanism of Hypochlorite-Induced Functionalization of Polymers toward Separating BFR-Containing Components from Microplastics.

Surface functionalization of polymers is significant for an emerging flotation technique for separation of microplastics toward the recycling of plastic wastes. In this study, the hypochlorite-induced functionalization of polymers, including ABS, PMMA, PS, and PVC polymers, was intensively investigated. Afterward, its emerging application in flotation separation of microplastic mixtures was assessed based on a Box-Behnken design of the response surface methodology. The functionalization favorably induced decreases in the contact angle and zeta potential of polymers, suggesting hydrophilic and negatively charged surfaces. Particularly, the functionalization of ABS polymers was the most effective, leading to the obviously decreased contact angle (from 92.5° to 67.8°) and zeta potential (from -26.4 mV to -41.7 mV) at neutral condition. The major mechanism for these variations was the oxidation of the sp3-C and butenyl group by hydroxyl radical and the hydrolysis of cyano group, which introduced the hydroxyl, carboxyl, and amide groups and rough topographies on the surface of ABS polymers. Oxygen functionalities introduced on the surfaces of other polymers were far less than those of ABS polymers. This selectivity inspired us to apply the functionalization in flotation separation of ABS microplastics from microplastic mixtures. After functionalization, ABS microplastics showed a significantly decreased floatability in flotation tests since the hydrophilic surface was repulsive to the adhesion of air bubbles. An empirical model was built to optimize the separation efficiency using the overall desirability function. Under optimum conditions, ABS microplastics were efficiently separated, and their removal rate, recovery, and purity were 99.8%, 99.8%, and >99.9%, respectively. These findings provide significant insights into the mechanism of the functionalization of polymers and show a promising prospect for pollution control of plastic wastes.

Optimizing green ferrate (VI) modification towards flotation separation of waste polyvinylchloride and acrylonitrile-butadiene-styrene mixtures.

The recycling of waste plastics is of considerable significance with environmental and economic benefits, while available separation approaches have been considered as a major bottleneck for its widespread application. Thus, we proposed a simple method, flotation along with surface modification, to separate waste acrylonitrile-butadienestyrene and polyvinylchloride mixtures. Single-factor experiment was conducted to determine the critical parameters in surface modification. Surface response methodology using Box-Behnken Design was performed to optimize separation performance. The quadratic models were generated to predict the floatability of acrylonitrile-butadienestyrene and the difference between the floatability of polyvinylchloride and acrylonitrile-butadienestyrene. The model was also utilized to determine optimized conditions by desirability approaches. The optimized conditions were: concentration = 0.18 M, temperature = 75.00 °C, treatment time = 11.50 min along with stirring rate = 200 rpm. The efficient separation of acrylonitrile-butadienestyrene and polyvinylchloride was achieved, yielding recovery of 98.40% and purity of 98.43%. The experimental responses well agreed with predicted values, demonstrating the accuracy of the prediction model. The formed hydrophilic groups, coated iron oxide, and signs of corrosion were confirmed as the major mechanism for the selective surface hydrophilization of acrylonitrile-butadienestyrene. Consequently, this method is feasible for separation of waste acrylonitrile-butadienestyrene and polyvinylchloride mixtures, and can be expected to promote the sustainable recycling of waste plastics.