ABSTRACT
The circular economy (CE) is reasoned to organize complex systems supporting sustainable resilience by distinguishing between waste materials and economic growth. This is crucial to the electronic waste (e-waste) industry of developed countries, and e-waste operation management has become their top priority because e-waste contains toxic materials and valuable sources of elements. In the UK, although London Metropolitan city boasts an ambitious sustainable resilience target underlying the context of CE, practical implementation has yet to be feasible, with few investigations detailing if and how the existing target implications enable industrial and social-ecological sectors to continue their performance functionalities in the face of undesired disruptions. In this paper, a dynamic Bayesian Network (dynamic BN) approach is developed to address a range of potential risks. The existing London e-waste operation management is considered as an application of study for sustainable resilience development. Through the utilization of dynamic BN, a comprehensive analysis yields a Resilience Index (RI) of 0.5424, coupled with a StdDev of 0.01350. These metrics offer a profound insight into the intricate workings of a sustainable system and its capacity to swiftly rebound from unexpected shocks and disturbances. This newfound understanding equips policymakers with the knowledge needed to navigate the complexities of sustainable e-waste management effectively. The implications drawn from these in-depth analyses furnish policymakers with invaluable information, enabling them to make judicious decisions that advance the cause of sustainable e-waste management. The findings underscore that the absorptive capacity of a sustainable and resilient e-waste operation management system stands as the foremost defense mechanism against unforeseen challenges. Furthermore, it becomes evident that two pivotal factors, namely "diversifying the supply chain" and "enhancing supply chain transparency," play pivotal roles in augmenting the sustainability and resilience of e-waste operation management within the context of London's ambitious sustainability targets. These factors are instrumental in steering the trajectory of e-waste management towards a more sustainable and resilient future, aligning with London's aspirations for a greener and more eco-conscious future.
ABSTRACT
Ecosystems and human health are being negatively impacted by the growing problem of electrical waste, especially in developing countries. E-waste poses a significant risk to ecological systems because it can release a variety of hazardous substances into the environment, containing polybrominated diphenyl ethers and heavy metals, brominated flame retardants, polychlorinated dibenzofurans and polycyclic aromatic hydrocarbons, and dioxins. This review article provides a critical assessment of the toxicological consequences of e-waste on ecosystems and human health and data analyses from scientific journals and grey literature on metals, BFRs, PBDEs, PCDFs, and PAHs in several environmental compartments of commercial significance in informal electronic trash recycling. The currently available techniques and tools employed for treating e-waste are sustainable techniques such as bioremediation, chemical leaching, biological leaching, and pyrometallurgy have been also discussed along with the necessity of implementing strong legislation to address the issue of unregulated exports of electronic trash in recycling practices. Despite the ongoing hurdles, implementing environmentally sustainable recycling methods have the potential to address the detrimental impacts of e-waste and foster positive economic development.
ABSTRACT
TetrabromobisphenolA is a well-known member of the brominated flame retardant group and is widely used as a highly effective fire-retardant additive in electronic and electrical equipment. TBBPA is commonly found in various environmental sources and can be harmful to human health. This study presents a simple approach to preparing a magnetic nanocomposite, offering a straightforward method that results in consistent quality and low resource consumption. The nanocomposite has a high surface-to-volume ratio for the removal of tetrabromobisphenolA. Various characterization techniques, including XRD, FTIR, EDX, FESEM, VSM, TEM, and BET analyses were used to characterize the Fe-S nanoparticles and Fe-S/CuS. The results showed that Fe-S/CuS nanocomposite successfully removed over 97% of the initial TBBPA (15 mg L-1) under optimized conditions determined by RSM, such as a contact time of 15 min, pH of 7, Fe-S/CuS nanocomposite dosage of 0.69 g L-1, and salt concentration of 0.10%. The RSM analysis provided a second-order polynomial model with a confidence level of 93% (F = 29.58; p < 0.0001) to predict the TBBPA removal efficiency at various concentrations. In the adsorption kinetic studies, the second-order kinetic model provided the best fit for the experimental data. Additionally, Fe-S/CuS nanocomposite shows great potential for practical applications and environmental remediation efforts, making it a valuable asset for real-sample use in environmental settings.
ABSTRACT
Economic and environmental considerations have elucidated research interests on the best approach to managing electronic waste (e-waste), which has increasing social, environmental, and economic impacts. Proper e-waste managementis essential for resource recovery, environmental sustainability, and public health protection, and effective management of e-waste necessitates analytical techniques to assess and characterize their elemental composition. Despite expansive literature published on the topic of e-waste, there is scarce coverage of the various analytical techniques employed to characterize the inorganic contents of e-waste. This review discusses the various e-waste characterization techniques used in studies published between 2013 and 2023. Specifically, this review covers the analytical approaches employed to characterize the inorganic content of e-waste, the electronic devices or their components analyzed, the elements identified, the sample preparation methods adopted, and the merits and demerits of the analytical procedures. This review highlights the disparate approaches to e-waste characterization and the need for reliable and repeatable e-waste analysis and sample preparation methods.
Subject(s)
Electronic Waste , Recycling , Waste Management , Electronic Waste/analysis , Recycling/methods , Waste Management/methodsABSTRACT
Fine particular matter (PM2.5) and lead (Pb) exposure can induce insulin resistance, elevating the likelihood of diabetes onset. Nonetheless, the underlying mechanism remains ambiguous. Consequently, we assessed the association of PM2.5 and Pb exposure with insulin resistance and inflammation biomarkers in children. A total of 235 children aged 3-7 years in a kindergarten in e-waste recycling areas were enrolled before and during the Corona Virus Disease 2019 (COVID-19) lockdown. Daily PM2.5 data was collected and used to calculate the individual PM2.5 daily exposure dose (DED-PM2.5). Concentrations of whole blood Pb, fasting blood glucose, serum insulin, and high mobility group box 1 (HMGB1) in serum were measured. Compared with that before COVID-19, the COVID-19 lockdown group had lower DED-PM2.5 and blood Pb, higher serum HMGB1, and lower blood glucose and homeostasis model assessment of insulin resistance (HOMA-IR) index. Decreased DED-PM2.5 and blood Pb levels were linked to decreased levels of fasting blood glucose and increased serum HMGB1 in all children. Increased serum HMGB1 levels were linked to reduced levels of blood glucose and HOMA-IR. Due to the implementation of COVID-19 prevention and control measures, e-waste dismantling activities and exposure levels of PM2.5 and Pb declined, which probably reduced the association of PM2.5 and Pb on insulin sensitivity and diabetes risk, but a high level of risk of chronic low-grade inflammation remained. Our findings add new evidence for the associations among PM2.5 and Pb exposure, systemic inflammation and insulin resistance, which could be a possible explanation for diabetes related to environmental exposure.
Subject(s)
COVID-19 , Electronic Waste , Environmental Exposure , Insulin Resistance , Lead , Particulate Matter , Humans , Child , Lead/blood , COVID-19/blood , COVID-19/epidemiology , Child, Preschool , Male , Female , Blood Glucose/analysis , Inflammation/blood , Recycling , HMGB1 Protein/blood , Insulin/blood , Air Pollutants , SARS-CoV-2ABSTRACT
Improper electronic waste management in the world especially in developing countries such as Iran has resulted in environmental pollution. Copper, nickel, and manganese are from the most concerned soil contaminating heavy metals which found in many electronic devices that are not properly processed. The aim of this study was to investigate the biological removal of copper, nickel, and manganese by Bacillus species isolated from a landfill of electronic waste (Zainal Pass hills located in Isfahan, Iran) which is the and to produce nanoparticles from the studied metals by the isolated bacteria. The amounts of copper, nickel, and manganese in the soil was measured as 1.9 × 104 mg/kg, 0.011 × 104 mg/kg and 0.013 × 104 mg/kg, respectively based on ICP-OES analysis, which was significantly higher than normal (0.02 mg/kg, 0.05 mg/kg, and 2 mg/kg, respectively. The minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of metals on the bacterial isolates was determined. The biosorption of metals by the bacteria was evaluated by inductively coupled plasma optical emission spectroscopy (ICP-OES). The metal nanoparticles were synthetized utilizing the isolates in culture media containing the heavy metals with the concentrations to which the isolates had shown resistance. X ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used for the evaluation of the fabrication of the produced metal nanoparticles. Based on the findings of this study, a total of 15 bacterial isolates were obtained from the soil samples. The obtained MICs of copper, nickel, and manganese on the isolates were 40-300 mM, 4-10 mM, and 60-120 mM, respectively. The most resistant isolates to copper were FM1 and FM2 which were able to bio-remove 79.81% and 68.69% of the metal, respectively. FM4 and FM5 were respectively the most resistant isolate to nickel and manganese and were able to bio-remove 86.74% and 91.96% of the metals, respectively. FM1, FM2, FM4, and FM5 was molecularly identified as Bacillus cereus, Bacillus thuringiensis, Bacillus paramycoides, and Bacillus wiedmannii, respectively. The results of XRD, SEM and EDS showed conversion of the copper and manganese into spherical and oval nanoparticles with the approximate sizes of 20-40 nm. Due to the fact that the novel strains in this study showed high resistance to copper, nickel, and manganese and high adsorption of the metals, they can be used in the future, as suitable strains for the bio-removal of these metals from electronic and other industrial wastes.
ABSTRACT
This study explored the redox-mediated changes in a lead (Pb) contaminated soil (900 mg/kg) due to the addition of solar cell powder (SC) and investigated the impact of biochar derived from soft wood pellet (SWP) and oil seed rape straw (OSR) (5% w/w) on Pb immobilization using an automated biogeochemical microcosm system. The redox potential (Eh) of the untreated (control; SC) and biochar treated soils (SC + SWP and SC + OSR) ranged from -151 mV to +493 mV. In SC, the dissolved Pb concentrations were higher under oxic (up to 2.29 mg L-1) conditions than reducing (0.13 mg L-1) conditions. The addition of SWP and OSR to soil immobilized Pb, decreased dissolved concentration, which could be possibly due to the increase of pH, co-precipitation of Pb with FeMn (hydro)oxides and pyromorphite, and complexation with biochar surface functional groups. The ability and efficiency of OSR for Pb immobilization were higher than SWP, owing to the higher pH and density of surface functional groups of OSR than SWP. Biochar enhanced the relative abundance of Proteobacteria irrespective of Eh changes, while the relative abundance of Bacteroidota increased under oxidizing conditions. Overall, we found that both OSR and SWP immobilized Pb in solar panel waste contaminated soil under both oxidizing and reducing redox conditions which may mitigate the potential risk of Pb contamination.
Subject(s)
Calcium Compounds , Charcoal , Lead , Oxidation-Reduction , Soil Microbiology , Soil Pollutants , Lead/analysis , Charcoal/chemistry , Soil Pollutants/analysis , Calcium Compounds/chemistry , Oxides/chemistry , Titanium/chemistry , Soil/chemistry , BacteriaABSTRACT
Introduction: Little is known on the association between cross-shift changes in pulmonary function and personal inhalation exposure to particulate matter (PM) among informal electronic-waste (e-waste) recovery workers who have substantial occupational exposure to airborne pollutants from burning e-waste. Methods: Using a cross-shift design, pre- and post-shift pulmonary function assessments and accompanying personal inhalation exposure to PM (sizes <1, <2.5 µm, and the coarse fraction, 2.5-10 µm in aerodynamic diameter) were measured among e-waste workers (n = 142) at the Agbogbloshie e-waste site and a comparison population (n = 65) in Accra, Ghana during 2017 and 2018. Linear mixed models estimated associations between percent changes in pulmonary function and personal PM. Results: Declines in forced expiratory volume in one second (FEV1) and forced vital capacity (FVC) per hour were not significantly associated with increases in PM (all sizes) among either study population, despite breathing zone concentrations of PM (all sizes) that exceeded health-based guidelines in both populations. E-waste workers who worked "yesterday" did, however, have larger cross-shift declines in FVC [-2.4% (95%CI: -4.04%, -0.81%)] in comparison to those who did not work "yesterday," suggesting a possible role of cumulative exposure. Discussion: Overall, short-term respiratory-related health effects related to PM exposure among e-waste workers were not seen in this sample. Selection bias due to the "healthy worker" effect, short shift duration, and inability to capture a true "pre-shift" pulmonary function test among workers who live at the worksite may explain results and suggest the need to adapt cross-shift studies for informal settings.
Subject(s)
Occupational Exposure , Particulate Matter , Respiratory Function Tests , Humans , Ghana , Male , Adult , Particulate Matter/analysis , Female , Electronic Waste/statistics & numerical data , Middle Aged , Inhalation Exposure/adverse effects , Inhalation Exposure/statistics & numerical data , Vital Capacity , Forced Expiratory Volume , Air Pollutants, Occupational/analysisABSTRACT
The effects of different contents of e-waste alloy on the microstructure and joint properties of Cu90PSn brazing filler metal was investigated during copper and copper brazing. Microstructure of base metal and brazing filler metal was studied with scanning electronic microscopy (SEM). The properties of brazing joint obtained by adding different electronic waste filler metal for smelting copper alloy were compared together. The results indicated that the fluidity of Cu90PSn brazing filler metal was weakened and the spreading property of Cu90PSn brazing filler metal was damaged after the addition of e-waste copper alloy. The structure of Cu90PSn brazing filler metal is mainly composed of (Cu), Cu3P and (Cu,Sn) compounds. When a small amount of electronic waste copper alloy is added, a trace amount of Fe in the brazing filler metal is distributed in the matrix structure of the filler metal in the form of solid solution. With the increase of copper alloys contents by smelting e-waste, Fe content in Cu90PSn brazing filler metal increases; the granular Fe3P phosphide changes into lamellar form. The Cu3P compound phase changes from continuous large orderly arrangement to discontinuous small block structure. Therefore, adding a trace amount of electronic waste copper alloy to the solder induction brazing copper/copper can obtain a uniform composition of the brazing structure. And the welding performance is not affected. However, As the content of e-waste smelted copper alloy continues to increase, the tensile strength shows a downward trend, which is attributed to the presence of brittle compound Fe3P in the joint.
ABSTRACT
Electronic waste recycling companies have proliferated in many countries due to valuable materials present in end-of-life electronic and electrical equipment. This article examined the business characteristics and management performance of Electronic Products Recycling Association (EPRA), a Canadian nationwide electronic product stewardship organization. The organization's annual performance reports, from 2012 to 2020, for nine Canadian provinces in which it currently operates were aggregated and analyzed. Temporal analysis using regression and Mann-Kendall tests were employed, and five characteristics of EPRA's business were analyzed, including e-waste products collected, number of drop-off locations, efforts to build public awareness, operating expenses, and growth of e-waste stewardship. Results show a decline in the amount of e-waste collected across the provinces, except in New Brunswick, which started its program in 2017. The Mann-Kendall test revealed declining temporal trends in most provinces. Although the collection/drop off sites and stewardship organizations increased astronomically over the study period in Canada, the amounts of e-waste collected decreased. We found that public awareness generally did not increase the amount of e-waste collected, and these campaigns only appeared to be effective in jurisdictions with good accessibility of e-waste recycling. Processing cost accounted for the majority of the e-waste management budget in Canada, and different factors affected the financial success of the stewards differently.
Subject(s)
Electronic Waste , Recycling , Waste Management , Recycling/methods , Canada , Waste Management/methodsABSTRACT
The depleting supply of natural sources of rare earth elements (REE) is a concern to many nations as demand for advanced technology is becoming vital for national security. In this communication, the recovery of dysprosium(III) from aqueous systems was exemplified by a modified phosphorylated chitosan (PCs/MB) prepared by the C-Mannich reaction of phosphorylated chitosan, glutaraldehyde, and 4-hydroxycoumarin in ethanolic solution. Batch adsorption studies achieved a maximum adsorption capacity (qmax) of 34 mg/g at 25 °C and pH = 5.4 for 2 h. Fourier Transform-Infrared Spectroscopy, elemental mapping, and quantitative analyses revealed ion-exchange mechanism with C6-phosphate and a synergistic complexation with the amino group between two hexose units of the chitosan chain confirming the correlation provided by the pseudo-second order kinetics (R2 = 0.9996), extrapolated mean free energy of adsorption (Eads) of 12.9 kJ/mol from the corrected Dubinin-Radushkevich isotherm, and the extrapolated enthalpy of adsorption (ΔH0ads) of -42.4 kJ/mol from the linearized Van't Hoff plot. Competitive adsorption with iron(II), cerium(III), and neodymium(III) demonstrated preferential removal of dysprosium(III) and complete exclusion of iron(II), which illustrates potential application in the separation of REE from electronic wastes.
Subject(s)
Chitosan , Dysprosium , Hydrogels , Chitosan/chemistry , Dysprosium/chemistry , Adsorption , Hydrogels/chemistry , Phosphorylation , Kinetics , Green Chemistry Technology , Water Pollutants, Chemical/chemistry , Water Pollutants, Chemical/isolation & purification , Hydrogen-Ion Concentration , Water Purification/methods , Spectroscopy, Fourier Transform Infrared , ThermodynamicsABSTRACT
This study investigates the potential of using gold nanoparticles (Au NPs) synthesized from e-waste as electrocatalysts for the methanol oxidation reaction (MOR), with the aim of applying them as an anode in alkaline direct methanol fuel cells (ADMFCs). The research addresses the pressing environmental challenge of e-waste disposal and explores the recycling of e-waste to obtain valuable materials for sustainable applications. Vulcan-supported gold nanoparticles (Aue-w/C NPs) are synthesized from gold coatings recovered from Intel Pentium 4 processor pins, demonstrating the feasibility of e-waste as electrocatalyst precursors. Comprehensive characterization techniques such as UV-Vis spectroscopy, high-resolution transmission and transmission electron microscopy (HR-TEM, TEM), selected area electron diffraction (SAED), scanning electron microscopy (SEM), and X-ray diffraction (XRD) are employed to evaluate the structural properties of the electrocatalyst. Electrochemical evaluation in 0.5 M KOH electrolyte by cyclic voltammetry reveals that the synthesized Aue-w/C NPs exhibit electrocatalytic activity (25.5 mA·mg-1Au) comparable to their commercially synthesized counterparts (30.1 mA·mg-1Au). This study highlights the potential for sustainable approaches in the production of electrocatalysts by utilizing e-waste as a source of valuable catalyst materials. It represents a pioneering effort in harnessing e-waste as a sustainable resource, offering new avenues for sustainable energy technologies while addressing environmental concerns and technological challenges in the field of ADMFCs.
ABSTRACT
A tannin-based adsorbent was synthesized by pomegranate peel tannin powder modified with ethylenediamine (PT-ED) for the rapid and selective recovery of palladium and gold. To characterize PT-ED, field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS-Mapping), and Fourier transform infrared spectroscopy (FT-IR) were used. Central composite design (CCD) was used for optimization. The kinetic, isotherm, interference of coexisting metal ions, and thermodynamics were studied. The optimal conditions, including Au (III) concentration = 30 mgL-1, Pd (II) concentration = 30 mgL-1, adsorbent mass = 26 mg, pH = 2, and time = 26 min with the sorption percent more than 99 %, were anticipated for both metals using CCD. Freundlich model and pseudo-second-order expressed the isotherm and kinetic adsorption of the both metals. The inhomogeneity of the adsorbent surface and the multi-layer adsorption of gold and palladium ions on the PT-ED surface are depicted by the Freundlich model. The thermodynamic investigation showed that Pd2+ and Au3+ ions adsorption via PT-ED was an endothermic, spontaneous, and feasible process. The maximum adsorption capacity of Pd2+ and Au3+ ions on PT-ED was 261.189 mgg-1 and 220.277 mgg-1, respectively. The probable adsorption mechanism of Pd2+ and Au3+ ions can be ion exchange and chelation. PT-ED (26 mg) recovered gold and palladium rapidly from the co-existing metals in the printed circuit board (PCB) scrap, including Ca, Zn, Si, Cr, Pb, Ni, Cu, Ba, W, Co, Mn, and Mg with supreme selectivity toward gold and palladium. The results of this work suggest the use of PT-ED with high selectivity and efficiency to recover palladium and gold from secondary sources such as PCB scrap.
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In this study, gold-reduced graphene oxide (Au@rGO) nanocomposite has been synthesized by repurposing electronic waste and dry batteries. This innovative approach involved utilizing the graphite rod from dry batteries to produce reduced graphene oxide (rGO), which was subsequently modified through the incorporation of gold nanoparticles obtained from recycled electronic waste. This methodology marks a significant breakthrough in electronic waste recycling, presenting a cost-effective and sustainable means of creating novel nanocomposites for applications in photocatalysis and adsorption, particularly in the removal of crystal violet (CV) from aqueous media. The synthesized Au@rGO nanocomposite was characterized using X-ray diffraction, scanning electron microscopy, energy dispersed X-ray, and N2 adsorption/desorption. Parameters that affect the adsorption and photocatalytic degradation of CV dye have been studied in detail. The optimal conditions for CV adsorption and photocatalytic degradation were pH of 10, equilibrium time of 30 min, CV concentration of 10 mg/L and adsorbent dosage of 40 mg. Furthermore, the isotherm and kinetics of CV removal were also studied. The removal of CV dye using adsorption and photocatalytic degradation techniques reached 95% and 99%, respectively. Consequently, the results showed that photocatalytic degradation of CV dye onto the mesoporous Au@rGO nanocomposite is more proper way than the adsorption technique for removing the CV dye from aqueous media. The designed photocatalyst has high efficiency and it can be reused and activated several times so it can be used in real water treatment applications.
ABSTRACT
The recovery of metals from solid waste for use as heterogeneous catalysts to activate peroxymonosulfate (PMS) for organic wastewater treatment is a promising, environmentally friendly and economical strategy. Herein, we present a facile and versatile strategy for upcycling copper (Cu) from waste printed circuit boards (PCBs) to Cu oxides supported on a three-dimensional carbon framework (10PCBs-Cu-TA) with the aid of tannic acid (TA). Compared to the PCBs-Cu synthesized without TA, introducing TA into 10PCBs-Cu-TA reduced Cu leaching, enhanced crystallinity, promoted electron transfer, and increased the number of oxygen vacancies. Moreover, 10PCBs-Cu-TA exhibited superior catalytic activity in activating PMS for the degradation of reactive brilliant blue KN-R, exceeding the activity of 10Cu-TA prepared using commercial Cu(NO3)2·3H2O. This enhanced performance may be attributed to the higher specific surface area and oxygen vacancies of 10PCBs-Cu-TA. The 10PCBs-Cu-TA/PMS system also exhibited broad catalytic universality and adaptability to various contaminants and water matrices. Quenching experiments, electron paramagnetic resonance analysis, and electrochemical measurements indicated that radical and non-radical processes jointly contributed to KN-R degradation. The proposed strategy for upcycling Cu from waste PCBs into functional materials provides novel insights into the utilization of solid waste and the development of PMS activators.
ABSTRACT
Unsustainable production and consumption are driving a significant increase in global electronic waste, posing substantial environmental and human health risks. Even in more developed nations, there is the challenge of low collection rates. In response, we integrate offline and online trading systems and design a material efficiency strategy for used cell phones. We propose a new multi-objective optimization framework to maximize profit, carbon emissions reduction, and circularity in the process of recycling and treatment. Considering multi-period, multi-product, multi-echelon features, as well as price sensitive demand, incentives, and qualities, we established a new multi-objective mixed-integer nonlinear programming optimization model. An enhanced, Fast, Non-Dominated Solution Sorting Genetic Algorithm (ASDNSGA-II) is developed for the solution. We used operational data from a leading Chinese Internet platform to validate the proposed optimization framework. The results demonstrate that the reverse logistics network designed achieves a win-win situation regarding profit and carbon emission reduction. This significantly boosts confidence and motivation for engaging in recycling efforts. Online recycling shows robust profitability and carbon reduction capabilities. An effective coordination mechanism for pricing in both online and offline channels should be established, retaining offline methods while gradually transitioning towards online methods. To increase the collection rate, it is essential to jointly implement a transitional strategy, including recycling incentives and subsidy policies. Additionally, elevating customer environmental awareness should be viewed as a long-term strategy, mitigating the cost of increasing collection rates during the market maturity stage (high collection rates).
Subject(s)
Cell Phone , Electronic Waste , Humans , Recycling/methods , Costs and Cost Analysis , CarbonABSTRACT
Polymers represent around 25% of total waste from electronic and electric equipment. Any successful recycling process must ensure that polymer-specific functionalities are preserved, to avoid downcycling. This requires a precise characterization of particle compounds moving at high speeds on conveyor belts in processing plants. We present an investigation using imaging and point measurement spectral sensors on 23 polymers including ABS, PS, PC, PE-types, PP, PVC, PET-types, PMMA, and PTFE to assess their potential to perform under the operational conditions found in recycling facilities. The techniques applied include hyperspectral imaging sensors (HSI) to map reflectance in the visible to near infrared (VNIR), short-wave (SWIR) and mid-wave infrared (MWIR) as well as point Raman, FTIR and spectroradiometer instruments. We show that none of the sensors alone can identify all the compounds while meeting the industry operational requirements. HSI sensors successfully acquired simultaneous spatial and spectral information for certain polymer types. HSI, particularly the range between (1600-1900) nm, is suitable for specific identification of transparent and light-coloured (non-black) PC, PE-types, PP, PVC and PET-types plastics; HSI in the MWIR is able to resolve specific spectral features for certain PE-types, including black HDPE, and light-coloured ABS. Fast-acquisition Raman spectroscopy (down to 500 ms) enabled the identification of all polymers regardless their composition and presence of black pigments, however, it exhibited limited capacities in mapping applications. We therefore suggest a combination of both imaging and point measurements in a sequential design for enhanced robustness on industrial polymer identification.
Subject(s)
Plastics , Polymers , Polymers/chemistry , Recycling , IndustryABSTRACT
As a steady stream of electronic devices being discarded, a vast amount of electronic substrate waste of petroleum-based nondegradable polymers is generated, raising endless concerns about resource depletion and environmental pollution. With coupled reagent (CR)-grafted artificial marble waste (AMW@CR) as functional fillers, polylactic acid (PLA)-based highly stretchable biodegradable green composite (AMW@CR-SBGC) is prepared, with elongation at break up to more than 250%. The degradation mechanism of AMW@CR-SBGC is deeply revealed. AMW@CR not only contributed to the photodegradation of AMW@CR-SBGC but also significantly promoted the water degradation of AMW@CR-SBGC. More importantly, AMW@CR-SBGC showed great potential as sustainable green electronic substrates and AMW@CR-SBGC-based electronic skin can simulate the perception of human skin to strain signals. The outstanding programmable degradability, recyclability, and reusability of AMW@CR-SBGC enabled its application in transient electronics. As the first demonstration of artificial marble waste in electronic substrates, AMW@CR-SBGC killed three birds with one stone in terms of waste resourcing, e-waste reduction, and saving nonrenewable petroleum resources, opening up vast new opportunities for green electronics applications in areas such as health monitoring, artificial intelligence, and security.
ABSTRACT
Human health effects can arise from unregulated manual disassembly of electronic waste (e-waste) and/or hydraulic fracturing fluid spills. There is limited literature on the effects of e-waste and hydraulic fracturing wastewater exposure on the male reproductive system. Thus, this proof-of-concept study begins to address the question of how wastewater from two potentially hazardous environmental processes could affect sperm quality. Therefore, three groups of eight-week-old adult mice were exposed (5 d/wk for 6 wks) via a mealworm (Tenebrio molitor and Zophabas morio) feeding route to either: (1) e-waste leachate (50% dilution) from the Alaba Market (Lagos, Nigeria); (2) West Virginia hydraulic fracturing flowback (HFF) fluid (50% dilution); or, (3) deionized water (control). At 24-hours (hr), 3 weeks (wk), or 9-wk following the 6-wk exposure period, cohorts of mice were necropsied and adverse effects/persistence on the male reproductive system were examined. Ingestion of e-waste leachate or HFF fluid decreased number and concentration of sperm and increased both chromatin damage and numbers of morphological abnormalities in the sperm when compared to control mice. Levels of serum testosterone were reduced post-exposure (3- and 9-wk) in mice exposed to e-waste leachate and HFF when compared to time-matched controls, indicating the long-term persistence of adverse effects, well after the end of exposure. These data suggest that men living around or working in vicinity of either e-waste or hydraulic fracturing could face harmful effects to their reproductive health. From both a human health and economic standpoint, development of prevention and intervention strategies that are culturally relevant and economically sensitive are critically needed to reduce exposure to e-waste and HFF-associated toxic contaminants.
Subject(s)
Electronic Waste , Hydraulic Fracking , Water Pollutants, Chemical , Male , Humans , Animals , Mice , Electronic Waste/adverse effects , Wastewater/toxicity , Nigeria , Semen/chemistry , Genitalia, Male , Water Pollutants, Chemical/toxicityABSTRACT
Chemical methods for the extraction and refinement of technologically critical rare earth elements (REEs) are energy-intensive, hazardous, and environmentally destructive. Current biobased extraction systems rely on extremophilic organisms and generate many of the same detrimental effects as chemical methodologies. The mesophilic methylotrophic bacterium Methylobacterium extorquens AM1 was previously shown to grow using electronic waste by naturally acquiring REEs to power methanol metabolism. Here we show that growth using electronic waste as a sole REE source is scalable up to 10 L with consistent metal yields without the use of harsh acids or high temperatures. The addition of organic acids increases REE leaching in a nonspecific manner. REE-specific bioleaching can be engineered through the overproduction of REE-binding ligands (called lanthanophores) and pyrroloquinoline quinone. REE bioaccumulation increases with the leachate concentration and is highly specific. REEs are stored intracellularly in polyphosphate granules, and genetic engineering to eliminate exopolyphosphatase activity increases metal accumulation, confirming the link between phosphate metabolism and biological REE use. Finally, we report the innate ability of M. extorquens to grow using other complex REE sources, including pulverized smartphones, demonstrating the flexibility and potential for use as a recovery platform for these critical metals.