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Plastic waste poses a critical environmental challenge for the world. The proliferation of waste plastic coffee pods exacerbates this issue. Traditional disposal methods such as incineration and landfills are environmentally unfriendly, necessitating the exploration of alternative management strategies. One promising avenue is the pyrolysis in-line reforming process, which converts plastic waste into hydrogen. However, traditional pyrolysis methods are costly due to inefficiencies and heat losses. To address this, for the first time, our study investigates the use of microwave to enhance the pyrolysis process. We explored microwave pyrolysis for polypropylene (PP), high-density polypropylene (HDPE), and waste coffee pods, with the latter primarily comprising polypropylene. Additionally, catalytic ex-situ pyrolysis of coffee pod pyrolysis over a nickel-based catalyst was investigated to convert the evolved gas into hydrogen. The single-stage microwave pyrolysis results revealed the highest gas yield at 500 °C for HDPE, and 41 % and 58 % (by mass) for waste coffee pods and polypropylene at 700 °C, respectively. Polypropylene exhibited the highest gaseous yield, suggesting its readiness for pyrolytic degradation. Waste coffee pods uniquely produced carbon dioxide and carbon monoxide gases because of the oxygen present in their structure. Catalytic reforming of evolved gas from waste coffee pods using a 5 % nickel loaded activated carbon catalyst, yielded 76 % (by volume) hydrogen at 900 °C. These observed results were supported by elemental balance analysis. These findings highlight that two-stage microwave and catalysis assisted pyrolysis could be a promising method for the efficient management of waste coffee pods, particularly for producing clean energy.
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Café , Hidrogênio , Micro-Ondas , Polietileno , Polipropilenos , Pirólise , Polipropilenos/química , Hidrogênio/química , Café/química , Catálise , Polietileno/química , Eliminação de Resíduos/métodosRESUMO
"White pollution" is regarded as one of the most serious problems in the natural environment. Thus greener recycling of plastic waste has attracted significant efforts in recent research. In this study, to kill two birds with one stone, a series of porous carbon nanobulks (PCNs) were synthesized from the pyrolysis of plastic waste (polyethylene terephthalate, PET) and inorganic salt (including NaHCO3, Na2CO3, NaCl, and ZnCl2) for sulfadiazine (SDZ) degradation via peroxymonosulfate (PMS) activation. PCNs-1 (co-calcinated from PET and NaHCO3) with a large number of CO and COOH active sites, which were in favor of PMS activation and electron transfer during the catalytic process, had shown the best catalytic activity for SDZ degradation. Significantly, PCNs-1 exhibited excellent universality, adaptability, and stability. The degradation pathways of SDZ were identified by the total content of organic carbon (TOC), and high-resolution mass spectrometry (HR-MS). The possible mechanism was proposed according to the anion effect, quenching experiments, electron paramagnetic resonance (EPR), and electrochemical analysis, indicating that radical (OH, SO4-, O2-) and non-radical (1O2 and e) species were the catalytically active species for SDZ decomposition in the PCNs-1/PMS system. Moreover, Ecological Structure-Activity-Relationship Model (ECOSAR) program and wheat seed cultivation experiments clearly demonstrated that the biotoxicity of SDZ could be effectively reduced by the PCNs-1/PMS system. Here we successfully upcycled plastic waste into high-value materials for efficient water decontamination.
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We report the standoff/remote identification of post-consumer plastic waste by utilizing a low-cost and compact standoff laser-induced breakdown spectroscopy (ST-LIBS) detection system. A single plano-convex lens is used for collecting the optical emissions from the plasma at a standoff distance of 6.5 m. A compact non-gated Czerny-Turner charge-coupled device (CCD) spectrometer (CT-CCD) is utilized to analyze the optical response. The single lens and CT-CCD combination not only reduces the cost of the detection system by tenfold, but also decreases the collection system size and weight compared to heavy telescopic-based intensified CCD systems. All the samples investigated in this study were collected from a local recycling plant. All the measurements were performed with only a single laser shot which enables rapid identification while probing a large number of samples in real time. Furthermore, principal component analysis has shown excellent separation among the samples and an artificial neural network analysis has revealed that plastic waste can be identified within â¼10 ms only (testing time) with accuracies up to â¼99%. Finally, these results have the potential to build a compact and low-cost ST-LIBS detection system for the rapid identification of plastic waste for real-time waste management applications.
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Cladosporium and Epicoccum are cosmopolitan fungi of the class Dothideomycetes with few cultured and genomic representatives. Here, we report draft reference genome sequences of Epicoccum sp. F181 (GenBank accession number JAJSLS01), Cladosporium sp. F165 (JAJSLR01), and F190 (JAJSLT01) isolated from recycling and waste management facilities in New Zealand.
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Plastic products are now essential commodities, yet their widespread disposal leads to environmental and human health effects, particularly in developing nations. Therefore, developing nations require comprehensive studies to assess the current state of plastic and plastic waste production to enhance plastic waste management practices. This review analyzes the import and export of plastic and the production of plastic waste in Rwanda, aiming to improve waste management practices. This review used open-access papers, reports, and websites dealing with plastic waste management. In this review, 58 articles from the Web of Science and 86 from other search engines were consulted to write this review. The findings revealed that the daily estimated plastic waste produced per person ranges between 0.012 and 0.056 kg. The estimated amount of plastic waste generated per person per year in Rwanda could be between 4.38 and 20.44 kg. Plastic waste accounts for between 1 and 8% of the total municipal solid waste produced per person per day in the country, which ranges from 219 to 255.5 kg. The average annual amount of imported plastics could reach 568.2881 tons, whereas the average quantity of exported plastics could reach 103.7414 tons. This shows that plastic management practices have not yet adopted technically advanced or improved practices, which should concern efforts to protect our environment. This study suggests approaches that can vastly improve plastic waste management and potentially open massive opportunities for the people of Rwanda.
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Plastics incorporate diverse additives, including primary antioxidants with a typical amount between 0.05 to 3 wt.%, to enhance plastics functionality and durability, preventing their oxidation and maintaining their mechanical properties. While these antioxidants offer substantial benefits, their degradation can significantly impact plastic pyrolysis by changing the pyrolysis oil product distribution. Understanding the intricate distribution of decomposition products resulting from pyrolysis is essential yet often overlooked. This study delved into the analysis of the decomposition of common primary antioxidants, namely, Irganox 1010, Irganox 1076, and butylated hydroxytoluene (BHT), utilizing both one-dimensional gas chromatography coupled with a quadruple mass spectrometer (GC-MS) and two-dimensional gas chromatography equipped with flame ionization detector and time-of-flight mass spectrometer (GC×GC-FID/TOF-MS). This study showed that GC×GC-FID/TOF-MS provided a more detailed characterization of the pyrolysis product distribution of primary antioxidants used in plastics in comparison to GC-MS. For each of the antioxidants, using the GC×GC-FID/TOF-MS analytical approach enhanced the identification of degradation products at least fivefold. Furthermore, GC×GC-FID/TOF-MS identified products of more chemical classes than GC-MS. For instance, compounds from 14 chemical classes were identified from GC×GC-FID/TOF-MS in the pyrolysis of Irganox 1010, whereas only 9 chemical classes were identified in GC-MS. Olefins were the major chemical class for both Irganox 1010 and Irganox 1076 in the decomposition process, accounting for 23.25 wt.% and 20.76 wt.%, respectively. Ketones were the major chemical class in the case of BHT, having a 6.68 wt.% yield. This research enhanced the understanding of the decomposition of primary antioxidant and their product distribution during pyrolysis and shed light on the potential necessity for using two-dimensional gas chromatography.
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The laser-based powder bed fusion of polymers (PBF-LB/P) process often utilizes a blend of powders with varying degrees of degradation. Specifically, for polyamide 12, the traditional reuse schema involves mixing post-processed powder with virgin powder at a predetermined ratio before reintroducing it to the process. Given that only about 15% of the powder is utilized in part production, and powders are refreshed in equal proportions, there arises a challenge with the incremental accumulation of material across build cycles. To mitigate the consumption of fresh powder relative to the actual material usage, this study introduces the incorporation of recycled material into the PBF-LB/P process. This new powder reuse schema is presented for the first time, focusing on the laser sintering process. The characteristics of the recycled powder were evaluated through scanning electron microscopy, differential scanning calorimetry, X-ray diffraction, particle size distribution, and dynamic powder flowability assessments. The findings reveal that waste powders can be effectively reused in PBF-LB/P to produce components with satisfactory mechanical properties, porosity levels, dimensional accuracy, and surface quality.
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Lasers , Polímeros , Pós , Reciclagem , Reciclagem/métodos , Polímeros/química , Tamanho da Partícula , Microscopia Eletrônica de Varredura , Difração de Raios X , Varredura Diferencial de Calorimetria , Gerenciamento de Resíduos/métodosRESUMO
The Pew Charitable Trust's 2020 report 'Breaking the Plastic Wave', indicates that existing technologies could support an 80% reduction in plastic leakage relative to business as usual by 2040. Therefore, South Africa became the first country to work with the Pew Charitable Trust and Oxford University to test and apply 'Pathways', a modelling framework and software tool which stemmed and evolved from the Pew report, at country level. The tool calculates the flows of plastics in the economy and the impact of various strategies to reduce future plastic pollution. The Scenario Builder within the Pathways tool allows the user to optimise flows in the plastics value chain to satisfy a set of defined objectives in order to achieve an optimal solution. Three major findings have emerged from the application of Pathways at country level for South Africa. Firstly, plastic pollution is set to almost double by 2040 if no interventions are implemented. Secondly, meeting the newly legislated extended producer responsibility (EPR) targets set for plastic packaging can avoid 33% of projected total pollution over the period of 2023-2040. Lastly, an optimal system change can avoid 63% of total plastic pollution over the period 2023-2040. Thus, applying Pathways at country level in South Africa has proven to be valuable by setting a baseline against which progress towards reducing plastic pollution can be measured; determining the outcome of meeting the legislated EPR targets over time, and informing policy decisions by allowing users to model different scenarios towards an optimal system change scenario.
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Plastic pollution is becoming increasingly severe and is attracting global attention. One of its consequences is the recent discovery of micropollutant discharge into water, with Bisphenol A (BA-MP) being a typical example. This study utilizes an advanced oxidation process based on Pt-doped ZnO photocatalyst to remove BA-MP. Health concerns related to the release of BA-MP from plastic waste are discussed. Besides, the results of the photodegradation experiment show that the Pt-ZnO photocatalyst can remove 94.1% of BA-MP within 60 min when exposed to solar light. Moreover, after five reuse cycles, Pt-ZnO retains a high BA-MP removal efficiency of 71.2%, and its structure remains largely unchanged compared to the original material. The removal efficiency of BA-MP leaching from plastic waste was measured at 98.8%, confirming the suitability of Pt-ZnO for the treatment of micropollutants. Furthermore, this study also highlights the prospects and challenges of using Pt-ZnO for the treatment of micropollutants discharged from plastic waste.
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Compostos Benzidrílicos , Fenóis , Fotólise , Plásticos , Platina , Poluentes Químicos da Água , Óxido de Zinco , Compostos Benzidrílicos/química , Óxido de Zinco/química , Fenóis/química , Catálise , Plásticos/química , Poluentes Químicos da Água/química , Platina/químicaRESUMO
Excessive production of waste polyethylene terephthalate (PET) poses an ecological challenge, which necessitates developing technologies to extract the values from end-of-life PET. Upcycling has proven effective in addressing the low profitability of current recycling strategies, yet existing upcycling technologies operate under energy-intensive conditions. Here we report a cascade strategy to steer the transformation of PET waste into glycolate in an overall yield of 92.6% under ambient conditions. The cascade approach involves setting up a robust hydrolase with 95.6% PET depolymerization into ethylene glycol (EG) monomer within 12 h, followed by an electrochemical process initiated by a CO-tolerant Pd/Ni(OH)2 catalyst to convert the EG intermediate into glycolate with high Faradaic efficiency of 97.5%. Techno-economic analysis and life cycle assessment indicate that, compared with the widely adopted electrochemical technology that heavily relies on alkaline pretreatment for PET depolymerization, our designed enzymatic-electrochemical approach offers a cost-effective and low-carbon pathway to upgrade PET.
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Técnicas Eletroquímicas , Polietilenotereftalatos , Polietilenotereftalatos/química , Catálise , Etilenoglicol/química , Poliésteres/química , Reciclagem , Hidrolases/químicaRESUMO
Plastic waste management has received significant attention in recent decades due to the urgent global environmental crisis caused by plastic pollution. The versatile and durable nature of plastic has led to its widespread usage across various sectors. However, its nonbiodegradable nature contributes to unsustainable production practices, leading to extensive landfill usage and posing threats to marine ecosystems and the food chain. To address these environmental concerns, numerous challenges have been recently addressed through investigating alternative approaches for disposing of plastic waste, with the construction sector emerging as a promising option. Incorporating plastic waste materials into concrete not only offers economic benefits but also provides a valid alternative to conventional disposal methods. This paper presents the results of different experimental studies, some of them available in the literature and others new, discussing the feasibility of integrating plastic waste into concrete and its impact on mechanical properties. The influence of different sizes, natures, treatments, and percentages of plastic waste in the concrete mixtures is dealt with in order to provide further data for helping to understand the nonunivocal results in the literature, under the conviction that only further observations can help to understand the mechanics of concrete with plastic aggregates. The experimental investigation highlighted that one parameter that is better than others and can be considered to compare different experimental investigations is the variation in weight (due to the effective volume of plastics in the mix), determining a sort of increasing of porosity that degrades the mechanical characteristics. However, this seems inconsistent in some cases. Therefore, the need for further research is highlighted to refine production methods and optimize mix designs.
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The escalating use of plastics in agriculture, driven by global population growth and increasing food demand, has concurrently led to a rise in Agricultural Plastic Waste (APW) production. Effective waste management is imperative, prompting this study to address the initial step of management, that is the quantification and localization of waste generated from different production systems in diverse regions. Focused on four Southern European countries (Italy, Spain, Greece, and Portugal) at the regional level, the study uses Geographic Information System (GIS), land use maps, indices tailored to each specific agricultural application and each crop type for plastic waste mapping. Furthermore, after the data was employed, it was validated by relevant stakeholders of the mentioned countries. The study revealed Spain, particularly the Andalusia region, as the highest contributor to APW equal to 324,000 tons per year, while Portugal's Azores region had the lowest estimate equal to 428 tons per year. Significantly, this research stands out as one of the first to comprehensively consider various plastic applications and detailed crop cultivations within the production systems, representing a pioneering effort in addressing plastic waste management in Southern Europe. This can lead further on to the management of waste in this area and the transfer of the scientific proposition to other countries.
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Waste plastics bring about increasingly serious environmental challenges, which can be partly addressed by their interconversion into valuable compounds. It is hypothesized that the porosity and acidity of a zeolite-based catalyst will affect the selectivity and effectiveness, enabling a controllable and selective conversion of polyethylene (PE) into gas-diesel or lubricating base oil. A series of embryonic, partial- and well-crystalline zeolites beta with adjustable porosity and acidity are prepared from mesoporous SBA-15. The catalysts and catalytic systems are studied with nuclear magnetic resonance (NMR), X-ray diffraction (XRD), and adsorption kinetics and catalytic reactions. The adjustable porosity and acidity of zeolite-beta-based catalysts achieve a controllable selectivity toward gas-diesel or lubricating base oil for PE cracking. With a catalyst with mesopores and appropriate acid sites, a fast escape and reduced production of cracking of intermediates are observed, leading to a significant fraction (88.7%) of lubricating base oil. With more micropores, a high acid density, and strong acid strength, PE is multiply cracked into low carbon number hydrocarbons. The strong acid center of the zeolite is confirmed to facilitate significantly the activation of hydrogen (H2), and, an in situ ammonia poisoning strategy can significantly inhibit hydrogen transfer and effectively regulate the product distribution.
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Non-governmental organizations (NGOs) play a critical role in addressing solid waste management (SWM) challenges in remote mountain communities, including the ecologically fragile Himalayan region. This study evaluates the impact of Healing Himalayas, an NGO, in Rakchham village, Himachal Pradesh, India. The objectives were to evaluate the effectiveness of Healing Himalayas' decentralized SWM model in promoting stakeholder engagement and resource recovery, assess the role of collaborations between local authorities and the NGO in financing waste management practices, investigate the influence of tourism and seasonal variations on solid waste generation patterns and waste management practices in Rakchham, and material recovery facilities, followed by glass (36.7%), paper/cardboard (18.4%) and metal (4.1%). A fee-based system involving the local village council funded waste operations. Waste generation exhibited significant seasonal fluctuations, with tourism influxes driving increased volumes. Healing Himalayas' initiatives promoted community participation, with over 15 awareness workshops conducted. Key challenges included limited financial resources, inadequate infrastructure, lack of advanced treatment facilities and need for context-specific solutions like efficient wet waste management in cold climates. The study highlights Healing Himalayas' decentralized model's success in fostering stakeholder engagement, behavioural change and resource recovery. The findings inform effective strategies for NGO-led waste management initiatives tailored to remote Himalayan communities.
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The standard techniques for monitoring beach litter focus on the litter that is accumulated on beaches. Therefore, the underwater bathing area is usually overlooked. Our study aims to start the discussion about the litter in the bathing area, an important connection between the exposed beach and the ocean. We aimed to compare sampling methodologies between the underwater bathing area and the exposed beach. We highlighted litter's similarities and differences regarding the amount, material, possible sources, and interaction with the biota. We also performed a brand audit on the underwater bathing area litter. In the underwater region, 106 items were collected while 1706 items were collected from the exposed beach region. Plastic was the dominant type of material in both sites, exposed beach (89.92 %) and bathing area (83.96 %). The litter's possible source was different. In the underwater bathing area was more related to food packages (couscous, rice). On the other hand, litter on the exposed beach was associated with beach use (single-use plastic such as plastic cups). The brand audit identified 21 companies, whereby most brands were Brazilian and food-related. Regarding interactions with the biota, the litter in the bathing area had more bio-fouling (87.73 %) than the litter collected on the exposed beach (10.00 %). Information about bathing area litter can be useful to draw different management strategies. Due to the differences in litter types and behavior between the two sites, the same mitigation strategies might not be equally efficient.
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Praias , Monitoramento Ambiental , Plásticos , Praias/estatística & dados numéricos , Monitoramento Ambiental/métodos , Plásticos/análise , BrasilRESUMO
High-density polyethylene (HDPE) waste poses a significant environmental challenge due to its non-biodegradable nature and the vast quantities generated annually. However, conventional recycling methods are energy-intensive and often yield low-quality products. Herein, HDPE waste is upcycled into anti-aging, superhydrophobic thin films suitable for outdoor applications. A two-layer spin-casting method combined with heating-induced crosslinking is utilized to produce an exceptionally rough superhydrophobic surface, featuring a root mean square (RMS) roughness of 50 nm, an average crest height of 222 nm, an average trough depth of -264 nm, and a contact angle (CA) of 148°. To assess durability, weathering tests were conducted, revealing the films' susceptibility to degradation under harsh conditions. The films' resistance to environmental factors is improved by incorporating a UV absorber, maintaining their hydrophobic properties and mechanical strength. Our research demonstrates a sustainable method for upcycling waste into high-performance, weather-resistant, superhydrophobic films.
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Microfiltration membranes derived from semi-crystalline polymers face various challenges when synthesized through the extrusion-casting technique, including the use of large quantities of polymer, long casting times, and the generation of substantial waste. This study focuses on synthesizing these membranes using spin-casting, followed by stretch-induced pore formation. Recycled high-density polyethylene (HDPE) and virgin polyethylene powder, combined with a calcium carbonate filler, were used as the source materials for the membranes. The influence of the polymer-filler ratio with and without stretching on the morphology, tensile strength, and water flow rate was investigated. Optimal conditions were determined, emphasizing a balance between pore structure and mechanical integrity. The permeable membrane exhibited a water flow rate of 19 mL/min, a tensile strength of 32 MPa, and a water contact angle of 126°. These membranes effectively eliminated suspended particles from water, with their performance evaluated against that of commercially available membranes. This research, carried out utilizing the spin-casting technique, outlines a synthesis route for microfiltration membranes tailored to semi-crystalline polymers and their plastic forms.
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Hundreds of millions of metric tons of plastic waste are generated globally every year. Processing waste into secondary raw material is preferred over energy production and landfilling. However, mechanical recycling generally deteriorates the properties of plastic waste limiting its range of potential applications. Nanocomposite fabrication is a solution to recycle plastic waste into value-added applications due to improved properties generated by nanomaterial reinforcement, however received little study. The aim of this review is to present the current status, identify research gaps and provide topics for further research of polymer nanocomposites prepared from plastic waste in respect to utilized materials, processing methods, enhanced properties, sustainability, economics, nanomaterial safety, and applications. It is found that morphological, mechanical, thermal, flame retardancy, physical, barrier, electrical and shielding properties of plastic waste can be enhanced with low loadings of different nanomaterials making them promising materials for various applications including electronic, shielding, thermal, packaging, filtration, and water treatment. Utilization of plastic waste instead of virgin polymers can be beneficial in respect to economics and sustainability, but the energy intensive and expensive production of the most nanomaterials, and the plastic waste pretreatment methods can negate these benefits. To enhance sustainability, further research should be conducted on utilization of energy friendly nanomaterials in plastic waste nanocomposites. Further research is needed also on polymer nanocomposite safety because of the unknow composition of the plastic waste and the potential for nanomaterial release during nanocomposite's life cycle. All in all, further research and national regulations and guidance are needed on virgin polymer and plastic waste nanocomposites.
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Hydrothermal carbonization (HTC) of single plastic polymers such as polyethylene terephthalate (PET) and polystyrene (PS) has not yet been explored on a large scale, particularly their thermal behavior, chemical transformations under subcritical conditions, and the energy properties of the resultant hydrochar. This study investigated these aspects by employing techniques, such as thermogravimetric analysis (TGA), Fourier transformed infrared spectroscopy (FTIR), elemental and calorific analysis. The results show that PET hydrochar has a superior energy densification (1.37) and energy yield (89 %) compared to PS hydrochar (1.13, 54 %). Hydrothermal carbonization modifies the chemical structure of the polymers by increasing the number of carbonyl groups (CO) in PET and forming new ones in PS, and by enhancing hydroxyl groups (OH) in PET while retaining them in PS. Both materials preserve their aromatic and aliphatic structures, with the introduction of alkenes groups (CC) in the PET hydrochar. PET hydrochar begins to decompose at lower temperatures (150-270 °C) than PS hydrochar (242-283 °C) but reaches higher peak temperatures (420-585 °C vs. 390-470 °C), with both types achieving similar burnout temperatures (650-800 °C). PET hydrochar recorded a higher activation energy (121-126 kJ/mol) than PS hydrochar (67-74 kJ/mol) with the Mampel first-order reaction model as the best fit.