Polyethylene Terephthalate Bottles Research Articles

Sustainability assessment of denim fabric made of PET fiber and recycled fiber from postconsumer PET bottles using LCA and LCC approach with the EDAS method.

The textile industry is under pressure to adopt sustainable production methods because its contribution to global warming is expected to rise by 50% by 2030. One solution is to increase the use of recycled raw material. The use of recycled raw material must be considered holistically, including its environmental and economic impacts. This study examined eight scenarios for sustainable denim fabric made from recycled polyethylene terephthalate (PET) fiber, conventional PET fiber, and cotton fiber. The evaluation based on the distance from average solution (EDAS) multicriteria decision-making method was used to rank scenarios according to their environmental and economic impacts, which are assessed using life cycle assessment and life cycle costing. Allocation, a crucial part of evaluating the environmental impact of recycled products, was done using cut-off and waste value. Life cycle assessments reveal that recycled PET fiber has lower freshwater ecotoxicity and fewer eutrophication and acidification impacts. Cotton outperformed PET fibers in human toxicity. Only the cut-off method reduces potential global warming with recycled PET. These findings indicated that recycled raw-material life cycle assessment requires allocation. Life cycle cost analysis revealed that conventional PET is less economically damaging than cotton and recycled PET. The scenarios were ranked by environmental and economic impacts using EDAS. This ranking demonstrated that sustainable denim fabric production must consider both economic and environmental impacts. Integr Environ Assess Manag 2024;20:2347-2365. © 2024 The Author(s). Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC).

Overcoming barriers to proactive plastic recycling toward a sustainable future

The plastics sector, accounting for a significant portion of global emissions, presents a challenge and an opportunity in achieving carbon neutrality. Despite Japan's commendable polyethylene terephthalate (PET) bottle recycling rates, most plastics are thermally recycled, creating environmental issues. This study proposes an evaluation framework to enhance recycling, aligned with end-user preferences and fostering a circular plastics economy. Employing a mixed-methods approach, this study conducts fieldwork including interviews with plastic recyclers and analysis of industry data. A weighted sum multicriteria analysis integrating end-user preferences, recycling effectiveness, and market dynamics is utilized. Systemic, process, and policy challenges were shown to hinder sustainable recycling practices, while varying willingness to pay, emission and cost reduction potentials, among acceptability and sectoral diversity informed priority plastic types for recycling. Multicriteria analysis showed that although PET is favored by end users, Polyoxymethylene (POM) emerges as a potential priority target for manufacturers and recyclers. Sensitivity analysis underscores the potential impact of establishing or enhancing willingness to pay (WTP) toward certain plastic types. Moreover, manufacturer and recycler evaluations suggest a broader willingness to recycle plastics than previously assumed. The proposed evaluation framework offers insights toward plastic recycling strategies. Policy interventions such as sustained subsidies for recyclers, market incentives leveraging WTP preferences, and technological advances, including chemical recycling and the broadening of plastic type recycling in line with user and manufacturer preferences, could all contribute to promoting sustainable plastic recycling practices.

Analytical and numerical calculation and simulation of heat transfer in a composite wall made of polyethylene terephthalate bottle

The dynamics of heat transfer in composite walls made of Polyethylene Terephthalate (PET) bottles is studied using the energy conservation model. Ten walls of different structures were studied, including two control walls made of compressed earth brick (CEB) and cementitious material, cement-sand brick (CSB) and eight composite walls made of PET bottles filled with thermal insulation and/or mechanical stabilisation materials. The model equation is solved analytically using the separation of variables method and numerically using the finite difference method, and they are confirmed using CASTEM finite element software. As boundary conditions, a constant temperature (Text) is applied at one end of the wall, and the constant temperature (T0) is applied at any other point at the initial time. The effect of PET bottles filling on the thermal behaviour of the wall was then carried out to determine the optimum design that would give the wall better thermal inertia. The results obtained with CASTEM is fairly in agreement with the results obtained analytically and numerically, with a maximum relative error closed to that of the spatial evolution and 3.310−2 for the temporal one. It is found that heterogeneous filling of PET bottles provides better thermal inertia at the wall.

Experimental and theoretical insights into bioethanol recovery: Valorizing waste PET bottles for sustainable pervaporation membranes

The use of bioethanol as an alternative source of fuel could solve energy and pollution concerns. However, its conventional recovery procedures make the overall process costly and energy intensive. Membrane-based pervaporation (PV) has gained significant attention in recent years. Most membranes that purify bioethanol are fabricated from conventional fossil-based polymers. This study presents the first work for biofuel separation by valorizing waste polyethylene terephthalate (PET) bottles into PV membranes. The performance of the membrane was characterized in terms of FTIR, XRD, TGA, WCA, SEM, and AFM and tested for a 10 wt% ethanol–water feed mixture at different temperatures. The mild hydrophobic character of PET allowed the PV membrane to achieve a separation factor of 10.45, a total flux of 1.7 kg m−2h−1, and a pervaporation separation index (PSI) of 18.72 at 45 °C. The recycled PET membrane (rPET) has higher mass transfer resistance for water compared to ethanol. The density functional theory (DFT) analysis confirms a stronger affinity of PET membrane towards ethanol than water. The results showed that rPET membranes have competitive performance compared to conventional fossil-based derived membranes. This study explores an energy-environment nexus approach, which could significantly contribute to achieving the key United Nations’ sustainable development goals.

Utilization of waste PET-derived metal–organic framework grafted polyaniline composite for heavy metal adsorption from aqueous solution

In this research, we used waste polyethylene terephthalate (PET) bottles as a source to develop an iron-based MOF-supported polyaniline (Fe-MOF@PANI) composite, which was then applied for the adsorptive removal of cadmium (Cd(II)) and lead (Pb(II)) ions from aqueous environment. A comprehensive characterization of the Fe-MOF@PANI composite was conducted using several analytical techniques including FTIR, PXRD, SEM, EDX with mapping, and XPS analysis, which provided significant insights into its functionality, crystalline structure, surface morphology, and elemental composition. The synthesized Fe-MOF exhibited a spindle-shaped morphology that was evenly distributed over the surface of the PANI composite, as confirmed by SEM analysis. Additionally, the porous characteristics of the Fe-MOF@PANI composite were proven through BET analysis. The Fe-MOF@PANI composite exhibited remarkable adsorption efficiencies for selected metal cations, achieving adsorption capacities of 143.36 mg/g and 258.59 mg/g for Cd(II) and Pb(II) ions, respectively. The findings of the isotherm and kinetic studies demonstrated that the adsorption process fitted well with Langmuir and pseudo-second-order kinetics, indicating that adsorption of both metal cations occurs in a monolayer formation and includes chemisorption mechanisms, respectively. This research paves the way for further development and application of post-functionalized PET-derived MOF adsorbents to remove Cd(II) and Pb(II) ions from water efficiently.

Efficient photoreforming of plastic waste using a high-entropy oxide catalyst

Simultaneous catalytic hydrogen (H2) production and plastic waste degradation under light, known as photoreforming, is a novel approach to green fuel production and efficient waste management. Here, we use a high-entropy oxide (HEO), a new family of catalysts with five or more principal cations in their structure, for plastic degradation and H2 production. The HEO shows higher activity than that of P25 TiO2, a benchmark photocatalyst, for the degradation of polyethylene terephthalate (PET) plastics in water. Several valuable products are produced by photoreforming of PET bottles and microplastics including H2, terephthalate, ethylene glycol and formic acid. The high activity is attributed to the diverse existence of several cations in the HEO lattice, lattice defects, and appropriate charge carrier lifetime. These findings suggest that HEOs possess high potential as new catalysts for concurrent plastic waste conversion and clean H2 production.

Impact of functionalized titanium oxide on anion exchange membranes derived from chemically modified PET bottles

The accessibility of newly affordable materials has drawn significant attention to the anion exchange membrane (AEM) technology. However, developing a high-performance AEM with excellent hydroxide conductivity and long-term durability is still challenging. The present work aims to improve the overall properties of AEMs synthesized by chemical modification of Polyethylene terephthalate (PET) bottles as the starting material. The modified PET structure was confirmed using IR, NMR, and HPLC-ESIMS analyses. AEMs were developed by incorporating quaternary ammonium (QA) functional groups into the modified PET structure, necessary for transporting anionic species (OH−). In addition, TiO2 nanoparticles grafted with silane coupling agents containing amine functional groups were synthesized via the sol-gel method and embedded in the polymer matrix. Then, the prepared nanocomposite membranes were thoroughly characterized, and the results displayed an overall improvement in the membrane's physicochemical properties. The composite membrane with 3wt% content of nanoparticle (NC3 %/M-PETm) showed remarkable conductivity, reaching 126 mS/cm at 80 °C, doubling the value of pristine membranes (64 mS/cm) while also displaying alkaline stability, retaining up to 92.2 % of conductivity after 20 days in harsh 2 M KOH at 80 °C. These results proved the suitability of these membranes for electrochemical energy applications. This innovative approach offers potential cost savings in preparing the new membranes while aligning with sustainable and circular economy principles.

Targeted aggregation of PETase towards surface of Stenotrophomonas pavanii for degradation of PET microplastics

Polyethylene terephthalate (PET) is one of the most widely used plastics, but its fragmentation into microplastics poses significant environmental challenges. The recycling of PET microplastics is hindered by their low solubility and widespread dispersion in the environment, making microbial in-situ degradation a promising solution. However, existing PET-degrading strains exhibited the limited effectiveness, primarily due to the diffusion of secreted hydrolases away from the PET surface. In this study, Stenotrophomonas pavanii JWG-G1 was engineered to achieve the targeted aggregation of PET hydrolase PETase on the cell surface by fusing it with an endogenous anchor protein. This approach aims to maximise the local concentration of PETase around PET, thereby increasing the overall rate of PET degradation. The PETase surface-aggregated system, S. pavanii/PaL-PETase, demonstrated the highest degradation efficiency, achieving 63.3 % degradation of low-crystallinity PET (lcPET) and 27.3 % degradation of high-crystallinity PET bottles (hcPET) at 30 °C. This represents the highest degradation rate reported for a displayed whole-cell system at ambient temperature. Furthermore, this system exhibited broad-spectrum degradation activity against various polyesters. These findings suggest that this system offers a promising, eco-friendly solution to PET and other polyester pollution, with potential implications for environmental bioremediation strategies.

Life Cycle Comparative Assessment of Polyethylene Terephthalate (PET) Plastic Bottles: A Case Study of Drinking Bottled Water in Ramathibodi Hospital, Thailand

In the current context where all sectors aim to promote sustainable development, hospitals, as large organizations with significant human interactions, face challenges in managing not only medical waste but also general waste such as water bottles. Improper management of these wastes can lead to environmental problems and high disposal costs. This study performed a life cycle assessment (LCA) of regular (petroleum-based) and alternative (bio-based) polyethylene terephthalate (PET) bottles used in Ramathibodi Hospital, Thailand, to identify effective strategies for mitigating environmental impacts. The assessment was divided into three scenarios: label-free bottles, bio-based bottles, and 100% recycling. The results indicate that using label-free bottles instead of conventional ones merely reduces environmental impacts by 2%. Transitioning to 30% and 100% bio-based PET can decrease greenhouse gas (GHG) emissions by 7 and 13 tons of CO2 eq per year, respectively. Currently, the hospital's PET bottles contribute 56.2 tons of CO2 eq annually. Health impacts associated with conventional PET bottles amount to 11.70 disability-adjusted life years (DALYs), a comprehensive measure that includes both mortality and morbidity. Meanwhile, 30% and 100% bio-based bottles reduce this to 7.35 and 4.87 DALYs, respectively. Achieving 100% recyclability in bottle management can cut GHG emissions from disposal processes by up to 90%. Moreover, combining the use of 100% bio-based PET bottles with 100% recycling can lower GHG emissions by up to 40% compared to current practices. These findings highlight the potential for significant environmental and health benefits through improved bottled water management strategies in hospitals.

Epoxy asphalt binder reinforced with waste polyethylene terephthalate (PET) for improving toughness

ABSTRACT The instinct brittleness of epoxy resin is one of the challenges to the durability of epoxy asphalt pavements, which may cause various failures, such as cracking, potholes and delamination. To improve the toughness of epoxy asphalts, polymer tougheners have been commonly introduced. On the other hand, the rapid accumulation of unrecycled end-of-life polyethylene terephthalate (PET) waste brings a serious environmental problem. Addressing this, the research aims to explore the use of recycled PET (rPET) as a value-added toughener for epoxy asphalt binders. To obtain this goal, waste PET bottles were cut into flakes and integrated into asphalt binders to prepare rPET modified epoxy asphalt binders. The effect of the rPET content on the phase-separated morphology, rotational viscosity and mechanical and thermal properties of epoxy asphalt binder was studied. Notably, rPET dissolved in the asphalt binder, preventing the occurrence of phase separation in the discontinuous phase of rPET modified epoxy asphalt binders. The addition of rPET increased the viscosity, dynamic modulus and the glass transition temperature (Tg) of epoxy of epoxy asphalt binder. Furthermore, the mechanical properties and low-temperature performance of epoxy asphalt binder were also augmented. Remarkably, with the addition of 3 wt% rPET, the toughness of epoxy asphalt binder increased by 48%.

Unraveling the Impact of Oxygen Vacancy on Electrochemical Valorization of Polyester Over Spinel Oxides.

Electrochemical upcycling of end-of-life polyethylene terephthalate (PET) using renewable electricity offers a route to generate valuable chemicals while processing plastic wastes. However, it remains a huge challenge to design an electrocatalyst with reliable structure-property relationships for PET valorization. Herein, spinel Co3O4 with rich oxygen vacancies for improved activity toward formic acid (FA) production from PET hydrolysate is reported. Experimental investigations combined with theoretical calculations reveal that incorporation of VO into Co3O4 not only promotes the generation of reactive hydroxyl species (OH*) species at adjacent tetrahedral Co2+ (Co2+ Td), but also induces an electronic structure transition from octahedral Co3+ (Co3+ Oh) to octahedral Co2+ (Co2+ Oh), which typically functions as highly-active catalytic sites for ethylene glycol (EG) chemisorption. Moreover, the enlarged Co-O covalency induced by VO facilitates the electron transfer from EG* to OH* via Co2+ Oh-O-Co2+ Td interaction and the following C─C bond cleavage via direct oxidation with a glyoxal intermediate pathway. As a result, the VO-Co3O4 catalyst exhibits a high half-cell activity for EG oxidation, with a Faradaic efficiency (91%) and productivity (1.02mmol cm-2 h-1) of FA. Lastly, it is demonstrated that hundred gram-scale formate crystals can be produced from the real-world PET bottles via two-electrode electroreforming, with a yield of 82%.

Environmental impact of waste plastic oil and hydrogen-enriched diesel engines: A comprehensive review on performance, combustion, and emissions

This review focuses on the sustainable use of waste plastic by converting it into waste plastic oil (WPO) through catalytic pyrolysis. The primary objective is to explore the potential of WPO, derived from used polyethylene terephthalate bottles, as an alternative fuel for diesel engines. This review also evaluates WPO's physical and chemical properties, revealing that it possesses fuel attributes similar to those of petroleum-based fuels. Catalytic pyrolysis is employed on a laboratory scale, using catalysts such as silica, Zeolite Socony Mobil-5 (ZSM-5), alumina, and kaolin to extract WPO from mixed waste plastics. However, direct use of WPO in diesel engines has shown drawbacks, including significant combustion delays and increased emissions. To address these issues, this review suggests blending WPO with diesel fuel rather than using it as a standalone fuel. Furthermore, the review explores hydrogen enrichment in WPO blends to improve combustion efficiency. Hydrogen enrichment enhances thermal efficiency and reduces environmental emissions, showing potential for improved performance and lower brake-specific fuel consumption. This review presents a comparative analysis of various WPO blends with hydrogen enrichment, highlighting the benefits of incorporating hydrogen to boost combustion and performance. Although promising, further research is needed to ensure the sustainability and effectiveness of WPO blends as a long-term energy source.

Determination of Diffusion Coefficients of Bisphenol A (BPA) in Polyethylene Terephthalate (PET) to Estimate Migration of BPA from Recycled PET into Foods

Bisphenol A (BPA) is a known substance that is found in food contact materials as an intentionally added as well as a non-intentionally added substance. Traces of BPA were found as a non-intentionally added substance in recycled PET (rPET). In 2023, the EFSA proposed a new TDI of 0.0002 µg/kg bw/d, which is lower than the previous (temporary) TDI of 4 µg/kg bw/d by a factor of 20,000. The TDI of 0.0002 µg/kg bw/d would translate for a default 60 kg person eating one kilogram of food into a migration limit of 0.012 µg/kg in the food. This very low migration limit is a challenge to measuring BPA levels in food. A solution is to use migration modeling to establish maximum concentrations in rPET for different food contact applications. Precise diffusion coefficients for BPA in PET were determined within this study by use of migration kinetics. In June 2024, the European Commission proposed a new migration threshold limit for BPA of 1 µg/kg, which should be understood as a detection limit. From the results of this study, it can be concluded that a BPA concentration in the PET bottle wall of 297 mg/kg (3% acetic acid), 255 mg/kg (10% ethanol), and 192 mg/kg (20% ethanol) after storage for 365 d at 25 °C is in compliance with the migration threshold limit of 1 µg/kg. These maximum concentrations are far above the measured BPA concentrations on rPET bottles in Europe between 2019 and 2023. Therefore, the new proposed migration threshold limit for BPA cannot be exceeded.

Conversion of PET bottles into carbonaceous adsorbents for Pb(II) removal from aqueous solutions via KOH activation

In this study, we present a novel approach to repurpose waste Polyethylene terephthalate (PET), a prominent contributor to global plastic usage, for the synthesis of efficient adsorbents via facial pyrolysis. The as-synthesized adsorbents were applied for the removal of lead (Pb(II)) ions in aqueous solution. Controlled batch experiments at pH 5 with 0.075 g of adsorbent at room temperature (20 °C) were conducted to measure Pb(II) adsorption capacities (mg/g) and fitted on isotherm models (Langmuir, Freundlich, and Temkin) and kinetics models (Pseudo-First order, Pseudo-Second order, and Elovich). Thermodynamic experiments conducted at four different temperatures (293 K, 303 K, 313 K, and 323 K) provided enthalpy, entropy, and Gibbs free energy change parameters, explaining the Pb(II) adsorption behaviors on PET-based adsorbents. The activation process involving KOH, followed by carbonization, yielded adsorbents with exceptional surface areas, pore volumes, and elevated oxygen contents (up to 22.8 %). The best adsorbent exhibited superior performance, achieving a maximum adsorption capacity of 219.7 mg/g within a rapid equilibrium time of 15 min. The adsorption behavior adhered well to the Langmuir isotherm model (R2 = 0.999) and Pseudo-Second Order kinetics model (R2 = 0.999). Furthermore, C600K600 displayed outstanding reusability, with negligible efficiency reduction (<5 %) even after five consecutive cycles. These results underscore the successful conversion of PET waste into a low-cost and highly effective adsorbent, offering a promising solution for sustainable waste management.

Impact of cold plasma and thermal treatment on the storage stability and shelf-life of pineapple juice: A comprehensive postharvest quality assessment

The primary concern regarding the pineapple juice processing industry is its insufficient stability. The goal of this investigation is to evaluate the storage stability and shelf life of cold plasma (CP) and thermally treated pineapple juice samples (S1, untreated; S2, optimized plasma-treated; S3, extreme plasma-treated; S4, thermally-treated) packed in glass (GL) and polyethylene terephthalate (PET) bottles at 5, 15, and 25°C. The color parameters increased with time and storage temperature. However, the bioactive substances decreased during storage for all the samples. Moreover, all the samples at elevated temperatures showed a higher degradation rate for bioactive compounds and color parameters. The changes in color parameter values across all samples showed zero-order kinetics, while the bioactive compounds followed a 1st-order kinetics. The application of various packing materials and storage temperatures had a significant impact (p < 0.05) on the microbiological, enzyme inactivation, and biochemical characteristics of the samples. However, there was an insignificant effect (p > 0.05) on the pH, acidity, and soluble solids. CP and thermally-treated samples reduced natural microbiota below the detection limit (<1-log CFU/mL). The sensory quality of S2, S3, and S4 samples remained above the acceptable limit (OA>5) for 120 d at 5 ℃. The shelf-life of the optimized CP-treated juice sample packed in GL bottles was 90, 50, and 25 days at 5, 15, and 25°C, respectively, based on AA≥20 mg/100 mL, OA≥5, ΔE*≤12, and microbial count≤6-log CFU/mL. In conclusion, CP is an effective non-thermal method that may extend the shelf life of pineapple juice packed in GL bottles by up to 90 days in refrigerated conditions (5 °C).

The evolution of cutinase Est1 based on the clustering strategy and its application for commercial PET bottles degradation

The rapid increase in global plastic consumption, especially the worldwide use of polyethylene terephthalate (PET), has caused serious pollution problems. Due to the low recycling rate of PET, a substantial amount of waste accumulates in the environment, which prompts a growing focus on enzymatic degradation for its efficiency and environmentally friendliness. This study systematically designed and modified a cutinase, Est1 from Thermobifida alba AHK119, known for its potential of plastic-degradation at high temperatures. Additionally, the introduction of clustering algorithms provided the ability to understand and modify biomolecules, to accelerate the process of finding the optimal mutations. K-means was further proceeded based on the positive mutations. After comprehensive screening for thermostability and activity mutation sites, the dominant mutation Est1_5M (Est1 with the mutations of N213M, T215P, S115P, Q93A, and L91W) exhibited satisfying degradation ability for commercial PET bottles. The results showed that Est1_5M achieved a degradation rate of 90.84% in 72 h, 65-fold higher than the wild type. This study offers reliable theoretical and practical support for the development of efficient PET-degrading enzymes, providing a reference for plastic pollution management.

Upcycling waste polyethylene terephthalate (PET) bottles into high-performance activated carbon for electrochemical desalination

Upcycling waste polyethylene terephthalate (PET) bottles has attracted intensive research interests. This simultaneously alleviates plastic pollution and achieves a waste-to-resource strategy. Waste PET water bottles were used to fabricate value-added activated carbon (AC) electrodes for capacitive deionization (CDI). The KOH activation temperature (greater than 700 °C) prominently affected the physi-chemical properties and desalination performance of PET-derived activated carbons (PET-AC). Profiting from a large Brunauer–Emmet–Teller specific surface area (1448 m2 g−1) with a good mesoporous structure (the ratio of the mesopore volume to the total pore volume was 41.3%), PET-AC-1000 (activated at 1000 °C) possessed a huge specific capacitance of 108 F g−1 for capacitive ion storage. Moreover, when utilized as the electrode material in single-pass CDI, PET-AC-1000 exhibited a maximum electrosorption capacity of 10.82 ± 0.11 mg g−1 and a low level of energy consumption (0.07 kWh mol−1), associated with good electrochemical charging-discharging cyclic stability. The results provide a promising facile approach to tackle the challenge of plastic pollution and promote the advancement of electrode materials for economic affordable and energy-efficient electrochemical desalination process, which meets the United Nations (UN) sustainable development goals (SDGs).

Ammonia-Borane Dependent Transfer Hydrogenation of Carboxylic Esters to Primary Alcohols.

Here, we present a user-friendly protocol that uses bench-stable NH3·BH3 (AB) as the hydrogen transfer agent for the reduction of both aromatic and aliphatic esters without an external catalyst and base, delivering a structurally diverse array of primary alcohols (80-98% yields). The broad functional-group tolerance (halogen, boronic ester, -NO2, -OH, etc.) under environmentally acceptable conditions implies high practical utility. Further, a tandem catalytic conversion of a plastic waste polyethylene terephthalate (PET) bottle to 1,4-benzenedimethanol including fatty esters into respective fatty alcohols was shown.

Innovative solutions for potential use of waste polyethylene terephthalate bottle cap as aggregates in concrete

Innovative solutions for potential use of waste polyethylene terephthalate bottle cap as aggregates in concrete

Electrocatalytic Upgrading of Plastic and Biomass-Derived Polyols to Formamide under Ambient Conditions.

Electrocatalytic upgrading of wasted plastic and renewable biomass represents a sustainable method to produce chemicals but is limited to carbohydrates, leaving other value-added chemicals, such as organonitrogen compounds, being scarcely explored. Herein, we reported an electrocatalytic oxidation strategy to transform polyethylene terephthalate (PET) plastic-derived ethylene glycol (EG) and biomass-derived polyols into formamide, in the presence of ammonia (NH3) over a tungsten oxide (WO3) catalyst. Taking EG-to-formamide as an example, we achieved a high formamide productivity of 537.7 μmol cm-2 h-1 with FE of 43.2 % at a constant current of 100 mA cm-2 in a flow electrolyzer with 12-h test, representing a more advantageous performance compared with previous reports for formamide electrosynthesis. Mechanistic understanding revealed that the cleavage of the C-C bond in the EG was facilitated by nucleophilic attack of in situ formed nitrogen radicals from NH3, with resultant C-N bond construction and eventually formamide production. Furthermore, this strategy can be extended to transformation of PET bottle and a series of biomass-derived polyols with carbon number from three (glycerol) to six (glucose), producing formamide with high efficiencies. This work demonstrates a sustainable upgrading strategy of plastic and biomass that may have implications to more value-added chemicals production beyond carbohydrates.