E-waste Burning Research Articles

Characterizing organophosphate esters and chlorinated paraffins in surface soils affected by diverse e-waste disassembling process in South China: Occurrence, distinct emission, and risk assessment

E-waste recycling activities are a crucial emission source of organic pollutants, posing potential risks to the surrounding environment and human health. To understand the potential impact related to diverse e-waste dismantling activities, we investigated two categories of popular flame retardants (i.e., organophosphate esters (OPEs) and chlorinated paraffins (CPs) and their resultant possible ecological risk in 53 surface soil samples from Qingyuan, a well-known e-waste recycling region in South China. Varied concentrations of ΣOPEs (20.5–8720 ng/g) and ΣCPs (920–16800 ng/g) were observed at diverse dismantling sites, while relatively low levels of ΣOPEs (6.13–1240 ng/g) and ΣCPs (14.8–2870 ng/g) were found in surrounding soils. These results indicated that primitive e-waste dismantling processes were the primary emission source of OPEs and CPs in the studied area, with e-waste dumping and manual dismantling being the most important emission sources for OPEs and CPs. More importantly, CPs could be degraded/transformed into more toxic intermediates via dechlorination and decarbonization during the burning of e-waste. Furthermore, our results indicated the potential ecological risks posed by OPEs and CPs related to e-waste recycling.

Flowing toxics: E-waste field work in the Palestinian-Israeli space

We draw on several emerging literatures on contamination and waste and our own fieldwork on e-waste contamination in a Palestinian-Israeli border space to describe a “flowing” approach to toxic phenomena. We use this term as a shorthand to underscore the particular complexities of the socio-material-biological node called “toxics,” and the corresponding epistemic, methodological, and moral demands of studying them. Some episodes from typical days of field work assessing the dispersal of heavy metals from sites of e-waste burning illustrate our claims. Even this attempt to use straightforward techniques to measure the presence of an object of apparent elemental materiality was continually permeated and unsettled by the inescapable flowiness of toxics. Their sources, generation processes and fates were mobile and multiscalar, remarkably patchy heterogeneous and contingent in ways that mattered. At issue was not (just) inadequate knowledge, but the inescapably relational biophysical and social nature of toxics; their entanglement not only with the technical means, processes and definitions that make them perceptible, but with the multiple and often disjunct social contexts that allow, inform, and motivate attention and access to toxics sites, and the production of knowledge from them.

Polycyclic aromatic hydrocarbons in PM2.5 from an e-waste source site and a receptor site in Southern China: Atmospheric transport and process implications

Polycyclic aromatic hydrocarbons (PAHs) are potential contaminants released from informal electronic waste (e-waste) recycling. PAHs in PM2.5 collected at a rural e-waste (source) site and a background (receptor) site in Southern China were measured. Seasonal variations and regional transport of PAHs were investigated, and their sources and atmospheric processes were implied. The median concentrations of ∑18PAHs at the e-waste site (13.7 ng/m3) were one order of magnitude higher than those at the background site (median = 1.54 ng/m3), indicating the informal e-waste dismantling was a significant source. The seasonal variations of PAH concentrations at the two sites were similar, exhibiting noticeably unimodal distributions in winter, predominantly associated with the strengthened e-waste dismantling activities. Three molecular diagnostic ratios (MDRs) can be collectively used as potential markers of field informal e-waste burning sources. The dispersion model revealed that regional atmospheric transport from this e-waste site was a source of PAHs in the background air. Some MDRs significantly changed at the background site compared to the source site but could not be explained by the lifetime and/or gas-particle partition of the isomers. The differences complied with recent theories about the multiphase reactivity and evaporation of PAHs on aerosols. It was proposed that in warm and humid climates, the losses of PAHs from PM2.5 were dominated by their phase separation or diffusion, which was n-octanol/water partition coefficient (KOW) dependent. This hypothesis was further supported by data in the literature.

Pollution of heavy metal threat posed by e-waste burning and its assessment of human health risk.

Improper treatment during recycling of e-waste materials by means of open burning is on the rise which has led to an increase in air pollution. This study looked at heavy metal concentrations, concentrations in relation to threshold values, and assessments of risk for noncarcinogenic and cancer risk threat. The Microwave Plasma-Atomic Emission Spectrometry (MP-AES 4210) series instrument of Agilent Technology, United States of America (USA), was used in analyzing heavy metal (Cd, Cu, and Pb) concentrations. The result of the analysis of the Kuka Bulukiya treatment point revealed that Pb has the highest mean concentration of 0.0693ppm, Cu 0.0525 parts per million (PPM), and Cd 0.0042ppm. The mean concentration at PRP Gidan Ruwa for Cd was found to be 0.0059ppm, Cu 0.0363ppm, and Pb 0.049ppm. The result of the adult and children population calculated shows that the hazard quotient (HQ) and hazard index (HI) values are not up to 1 in all the pathways (inhalation, ingestion, and dermal) at both treatment points (1.2 ˟ 10-4 and 9.8 ˟ 10-5) and (6.4 ˟ 10-4 and 5.9 ˟ 10-4), respectively. The cancer risk for Kuka Bulukiya 6 ˟ 10-10 and PRP G/Ruwa 5 ˟ 10-10 for adults and 7 ˟ 10-10 and 4 ˟ 10-10 for children were both lower than the threshold set for cancer risk by the United States Environmental Protection Agency (USEPA). This meant that both adults and children were not at risk of cancer and noncarcinogenic threat based on the assessment in this study. The study concluded that informal e-waste burning has substantially helped in the relatively high levels of air pollution identified in the treatment points and in turn posed environmental and public health concerns to people around the area. This study recommends that samples of the vegetable products at the PRP G/Ruwa treatment point should be investigated immediately and adequate restrictions and regulations should be enacted and enforced in order to safeguard the environment and the populace. There is need for caution from the authorities to avert the possible implications (e-waste extractors and the public) of being affected with noncarcinogenic or carcinogenic ailments over time.

Heavy metals in fish nearby electronic waste may threaten consumer's health. Examples from Accra, Ghana

Electronic waste sites are rich in heavy metals contained in electronic and electric equipment waste and pose a risk of pollution if metals enter in the environment nearby. The Korle lagoon, located in the center of Accra, is receiving waste effluents from industries, households and the adjacent e-waste burning site Agbogbloshie which is the biggest in the country. Thus, the risk of heavy metal contamination of the water body and subsequent uptake in the aquatic food chain is particularly relevant. Small-scale fishing, not entering the commercial chain, occurs in the lagoon despite its consideration of biologically dead. We assessed if the exposure to heavy metals through these fish consumption is posing higher health risks than fish sold on Ghanaian markets. Using ICP-MS technology, we quantified concentrations of As, Cd, Co, Cr, Cu, Hg, Ni, Pb and Zn in fish caught from the Korle Lagoon (Trachinotus ovatus, Mugil curema and Mugil cephalus) and compared them to fish from the Tema Newtown fishing market (Scomber colias, Pseudotolithus senegallus). Cobalt and lead concentrations, typical e-waste metals, were higher in fish from the Korle lagoon, even though they were of lower trophic level. Calculated risk indices revealed risk of elevated arsenic and mercury exposure, particularly through T. ovatus from the Korle lagoon, if consumed daily as it is common in the region. This study suggests the need of monitoring programs of Ghanaian catch, with a special focus in environmental risk areas like Korle lagoon to ensure human food safety.

Effect of Heavy Metals caused by E-waste Activities on Soil Samples, PM<sub>2.5</sub>, Human Fingernails, and Scalp Hair in Moradabad City, India

<p>E-waste is a popular name for electronic products nearing the end of their favorable life. Which ensuing in increased dangers of digital waste normally acknowledged as e-waste. Present study was aimed to find out the soil quality, air pollution and its relation to human health risk. Therefore, two study sites (SI and SII) were choised on the basis of various activities. PM<sub>2.5</sub> air samples had been gathered with the help of RDS after which were analyzed to heavy metals through ICP-MS. Objectives of the study, was to generate baseline data at the quantity of heavy metal cognizance in soil from two test sites. In rise, we measured the heavy metallic concentrations in scalp hair and fingernails to discover if there exists any relation among organic publicity and environmental. Hypertension, Hypoxemia and Asthma had been additionally decided for the evaluation of fitness parameters among the take a look at population. For this purpose, investigation also involved the collection of fingernails and scalp hair for heavy metal analysis (ICP-MS) from human subjects of two study sites. Results indicated that, except SI, SII had significant level of PM<sub>2.5</sub> and its heavy metal content. All soil indices which were employed to determine the level of pollution, indicates extreme level of metals at all the study sites. Therefore, local residents as well as workers, who were engaged in e-waste burning and industrial activities also had various levels of toxic metal concentrations in their scalp hair and fingernails. We concluded that the high levels of air pollution, containing toxic metal pollutants such as Pb, Zn, Cu and Ni released from e-waste burning activities, resulted in significant health risks for the exposed human population.It is recommended that environment of Moradabad City should be closely monitored by government agencies on routine basis. It was concluded that the toxic metal contamination imposed a negative influence on the environment, soil and human health.</p>

E-Waste in Africa: A Serious Threat to the Health of Children.

Waste electronic and electrical equipment (e-waste) consists of used and discarded electrical and electronic items ranging from refrigerators to cell phones and printed circuit boards. It is frequently moved from developed countries to developing countries where it is dismantled for valuable metals in informal settings, resulting in significant human exposure to toxic substances. E-waste is a major concern in Africa, with large sites in Ghana and Nigeria where imported e-waste is dismantled under unsafe conditions. However, as in many developing countries, used electronic and electrical devices are imported in large quantities because they are in great demand and are less expensive than new ones. Many of these used products are irreparable and are discarded with other solid waste to local landfills. These items are then often scavenged for the purpose of extracting valuable metals by heating and burning, incubating in acids and other methods. These activities pose significant health risks to workers and residents in communities near recycling sites. E-waste burning and dismantling activities are frequently undertaken at e-waste sites, often in or near homes. As a result, children and people living in the surrounding areas are exposed, even if they are not directly involved in the recycling. While toxic substances are dangerous to individuals at any age, children are more vulnerable as they are going through important developmental processes, and some adverse health impacts may have long-term impacts. We review the e-waste situation in Africa with a focus on threats to children’s health.

Temperature-dependent profiles of dioxin-like toxicants from combustion of brominated flame retardants

Literature provides detailed mechanisms underpinning the formation of a wide array of bromine (Br)-containing molecules with a prime focus on dioxin-like compounds. However, from a more applied point of view, the practical deployment of attained thermo-kinetic parameters remains inadequate in the absence of a robust kinetic model that connects bromine transformation at the molecular level with pertinent experimental observations. Herein and to fill in this gap, this study constructs a chemical kinetic model to account for the “homogenous gas phase” emission of Br-aromatic pollutants from the oxidative thermal decomposition of a monobromobenzene molecule (MBZ). The latter serves as a model compound for brominated flame retardants (BFRs) present in e-waste. The model consists of sub-mechanisms (that include reaction rate constants and thermochemical T-dependent functions) for HBr oxidation, combustion mechanism of C1-C6 species, bromine transformation, and synthesis of Br dioxin-like compounds. Reaction rate parameters were obtained for a large array of reactions that constitute the core of the model. For instance, the obtained activation energies for the initial pathways in the formation of brominated biphenyls reside in the range of ~15–45 kJ/mol. Considering oxidation of 5000 ppm MBZ in a plug flow reactor, the model reasonably predicts the temperature-dependent profiles (between 500 and 1200 °C at atmospheric pressure) of a few PBDD/Fs (i.e., polybrominated dibenzo-p-dioxins) isomers in reference to limited corresponding experimental measurements. Most Br dioxin-like compounds appear in the narrow temperature window of 600–1000 °C and achieve their highest abundance at molar yields in the range of 1.0–15 mmol/mol MBZ. A high load (100–120 mmol/mol MBZ) of brominated environmentally persistent free radicals (Br-EPFR) emerges and shifts from bromophenoxy radicals to bromocyclopentadienyl radicals around 700 °C. Oxidation of a 2-bromophenol molecule results in the formation of higher yields of Br-toxicants when compared with that of MBZ. The assembled model provides an informed hazards assessment into the potential emission inventories of Br-compounds in the gas phase at conditions encountered in real scenarios, such as open burning and primitive treatment of e-waste. Via an atomic-base understanding of the complex bromine chemistry and speciation, the model allows the underlying operational conditions that reduce the emission of Br-notorious pollutants to be surveyed and fine-tuned.

Gastric bioaccessibility and human health risks associated with soil metal exposure via ingestion at an E-waste recycling site in Kumasi, Ghana

Over 1000 people make a living by processing electronic and electrical waste (E-waste) and scrap metals for the recovery of valuable metals and integrated circuits at Dagomba Line, Kumasi, Ghana. The processing includes activities such as dismantling, open burning and open dumping of E-waste which can potentially release toxic metals into the environment and thus impact the health of recyclers and nearby residents. This study investigated the distribution of toxic metals (As, Cd, Cr, Cu, Hg, Ni, Pb, Sb and Zn) in surface soils at the E-waste recycling sites and determined the associated human health risk via ingestion incorporating bioaccessibility measurements. Metal concentrations in the activity sites were highly elevated, significantly higher than those in the surrounding area and exceeded international soil quality guidelines such as the Canadian soil quality guidelines for residential landuse and the Dutch Intervention Value. Bioaccessibility was high for Pb (70.8%), Cd (64.1%), Cu (62.3%) and Ni (53.6%) which could be credited to the existence of oxidized species as a result of the E-waste burning. Non-carcinogenic effects were unacceptably high (hazard indices > 1) at 14 out of 31 sites, and the cancer risk for arsenic for adult workers was greater than 1 × 10-5 at five of the sampling sites.

Effect of Particulate Matter Exposure on Respiratory Health of e-Waste Workers at Agbogbloshie, Accra, Ghana.

Background: Direct and continuous exposure to particulate matter (PM), especially in occupational settings is known to impact negatively on respiratory health and lung function. Objective: To determine the association between concentrations of PM (2.5, 2.5–10 and 10 µm) in breathing zone and lung function of informal e-waste workers at Agbogbloshie. Methods: To evaluate lung function responses to PM (2.5, 2.5–10 and 10 µm), we conducted a longitudinal cohort study with three repeated measures among 207 participants comprising 142 healthy e-waste workers from Agbogbloshie scrapyard and 65 control participants from Madina-Zongo in Accra, Ghana from 2017–2018. Lung function parameters (FVC, FEV1, FEV1/FVC, PEF, and FEF 25-75) and PM (2.5, 2.5–10 and 10 µm) concentrations were measured, corresponding to prevailing seasonal variations. Socio-demographic data, respiratory exposures and lifestyle habits were determined using questionnaires. Random effects models were then used to examine the effects of PM (2.5, 2.5–10 and 10 µm) on lung function. Results: The median concentrations of PM (2.5, 2.5–10 and 10 µm) were all consistently above the WHO ambient air standards across the study waves. Small effect estimates per IQR of PM (2.5, 2.5–10 and 10 µm) on lung function parameters were observed even after adjustment for potential confounders. However, a 10 µg increase in PM (2.5, 2.5–10 and 10 µm) was associated with decreases in PEF and FEF 25–75 by 13.3% % [β = −3.133; 95% CI: −0.243, −0.022) and 26.6% [β = −0.266; 95% CI: −0.437, 0.094]. E-waste burning and a history of asthma significantly predicted a decrease in PEF by 14.2% [β = −0.142; 95% CI: −0.278, −0.008) and FEV1 by 35.8% [β = −0.358; 95% CI: −0.590, 0.125] among e-waste burners. Conclusions: Direct exposure of e-waste workers to PM predisposes to decline in lung function and risk for small airway diseases such as asthma and COPD.

Soil pollution at a major West African E-waste recycling site: Contamination pathways and implications for potential mitigation strategies

Organic contaminants (polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and chlorinated paraffins (CPs)) and heavy metals and metalloids (Ag, Cd, Co, Cr, Cu, Hg, Ni, Pb, Sb, Zn) were analysed in surface soil samples from the Agbogbloshie e-waste processing and dumping site in Accra (Ghana). In order to identify which of the pollutants are likely to be linked specifically to handling of e-waste, samples were also collected from the Kingtom general waste site in Freetown (Sierra Leone). The results were compared using principal component analyses (PCA). PBDE congeners found in technical octa-BDE mixtures, highly chlorinated PCBs and several heavy metals (Cu, Pb, Ni, Cd, Ag and Hg) showed elevated concentrations in the soils that are likely due to contamination by e-waste. PCAs associated those compounds with pyrogenic PAHs, suggesting that burning of e-waste, a common practice to isolate valuable metals, may cause this contamination. Moreover, other contamination pathways, especially incorporation of waste fragments into the soil, also appeared to play an important role in determining concentrations of some of the pollutants in the soil. Concentrations of several of these compounds were extremely high (especially PBDEs, heavy metals and SCCPs) and in some cases exceeded action guideline levels for soil. This indicates that exposure to these contaminants via the soil alone is potentially harmful to the recyclers and their families living on waste sites. Many organic contaminants and other exposure pathways such as inhalation are not yet included in such guidelines but may also be significant, given that deposition from the air following waste burning was identified as a major pollutant source.

Toward Active Community Environmental Policing: Potentials and Limits of a Catalytic Model.

This paper offers a field tested community environmental policing model to address the pressing environmental management challenges of reducing e-waste burning in informal e-waste hubs, and enforcement against informal polluting industries more broadly. This is based on our intervention to reduce e-waste burning in a substantial informal e-waste hub in the West Bank, Palestine, a 45 km2 region in which an estimated 5-10 metric tonnes of cables are burnt daily, causing serious environmental and public health consequences. In analogous e-waste hubs in the global South, environmental management solutions have focused on economically attractive alternatives to replace cable burning or policies that integrate informal recyclers with formal e-waste management systems-achieving little success. Our paper describes a two-pronged intervention in Palestine's e-waste hub, which reduced e-waste burning by 80% through a combination of economically competitive cable grinding services and an "active" community environmental policing initiative that lowered barriers to and successfully advocated for governmental policing of e-waste burning. Our discussion of this intervention addresses the community environmental policing literature, which has documented few successes stories of real improvements to the enforcement of environmental violations. We argue that existing strategies have relied on "passive" approaches comprised of monitoring and reporting environmental violations to advocate for change. Our strategy offers a template to improve outcomes through a more "active" approach, moving from monitoring environmental violations through understanding the rationale and dynamics of violators, identifying environmental policing barriers, and implementing a feasible and persuasive strategy to overcome them.

Soil and sediment contamination by unsubstituted and methylated polycyclic aromatic hydrocarbons in an informal e-waste recycling area, northern Vietnam: Occurrence, source apportionment, and risk assessment

Improper processing activities of e-waste are potential sources of polycylic aromatic hydrocarbons (PAHs) and their derivatives, however, information about the environmental occurrence and adverse impacts of these toxic substances is still limited for informal e-waste recycling areas in Vietnam and Southeast Asia. In this study, unsubstituted and methylated PAHs were determined in surface soil and river sediment samples collected from a rural village with informal e-waste recycling activities in northern Vietnam. Total levels of PAHs and MePAHs decreased in the order: workshop soil (median 2900; range 870–42,000 ng g−1) > open burning soil (2400; 840–4200 ng g−1) > paddy field soil (1200; range 530–6700 ng g−1) > river sediment samples (750; 370–2500 ng g−1). About 60% of the soil samples examined in this study were heavily contaminated with PAHs. Fingerprint profiles of PAHs and MePAHs in the soil and sediment samples indicated that these pollutants were mainly released from pyrogenic sources rather than petrogenic sources. The emissions of PAHs and MePAHs in this area were probably attributed to uncontrolled burning of e-waste and agricultural by-products, domestic coal and biomass combustion, and traffic activities. Carcinogenicity and mutagenicity of PAHs in the e-waste workshop soils were significantly higher than those of the field soils; however, the incremental lifetime cancer risk of PAH-contaminated soils in this study ranged from 5.5 × 10−9 to 4.6 × 10−6, implying acceptable levels of human health risk. Meanwhile, concentrations of some compounds such as phenanthrene, anthracene, fluoranthene, benz[a]anthracene, and benzo[a]pyrene in several soil samples exceeded the maximum permissible concentrations, indicating the risk of ecotoxicological effects.

Emissions and Occupational Exposure Risk of Halogenated Flame Retardants from Primitive Recycling of E-Waste.

The production and usage of non-polybrominated diphenyl ether (PBDE) halogenated flame retardants (HFRs) have substantially increased after the ban of several PBDEs. This has resulted in widespread environmental occurrence of non-PBDE HFRs, further amplified by emissions from primitive recycling of obsolete electronics (e-waste). The present study conducted chamber experiments to characterize 15 HFRs (∑15HFR) from thermal treatment and open burning of typical e-waste. Emission factors of ∑15HFR from thermal treatment were 2.6 × 104-3.9 × 105 ng g-1, slightly higher than those from open burning (8.8 × 103-1.0 × 105 ng g-1). Greater output over input mass ratios of ∑15HFR were obtained in thermal treatment than in open burning. Particulate and gaseous HFRs dominated the emissions in thermal treatment and open burning, respectively, largely because of the different temperatures used in the two processes. Particulate HFRs were primarily affiliated with fine particles (Dp < 1.8 μm) peaking at 0.56-1.0 or 0.32-0.56 μm in both thermal treatment and open burning. Occupational exposure to most FRs was relatively low, but several PBDEs may pose potential health risk to workers in e-waste home-workshops. Potentially accruing emissions and health risks of non-PBDE HFRs from primitive recycling of e-waste remain a great concern.

Vertical profile of soil/sediment pollution and microbial community change by e-waste recycling operation

The present study aims to assess the effect of electronic waste (e-waste) recycling on microbial community and the underlying modulation mechanism. Core soil/sediment samples were collected from an abandoned e-waste burning site and neighboring farmland/stream sites in Guiyu, China. High concentrations and health risks of toxic heavy metals, particularly, Sb and Sn, and halogenated flame retardants (HFRs), including decabromodiphenyl ether (BDE 209) and decabromodiphenyl ethane (DBDPE) were mostly retained at the top surface layers of soils/sediments (0–30cm) after more than one year of natural vertical diffusion and microbe-facilitated biodegradation. Heavy metals, such as Ag, Cd, Cu, Pb, Sb, and Sn, played a critical role for the reduction of microbial diversity. This is the first study reporting the open burning of e-waste caused an obvious heat effect and enriched thermophilic/mesophilic microbes in local area. The acid washing during e-waste recycling process may result in the enrichment of acidophilic microbes. This investigation showed that e-waste processing operation resulted in not only severe pollution of the soils/sediments by various pollutants, but also reduction of microbial diversity that was difficult to self-store by the local ecosystem.

Assessment of air pollution caused by illegal e-waste burning to evaluate the human health risk

The onset of the 21st century has started a corresponding change in consumer lifestyles, resulting in the generation of a huge amount of the end-of-life electronics, known as e-waste. The e-waste recycling activities can pose a high risk to the environment and human health. We monitored air pollution levels (PM10) and heavy metal concentrations (Pb, Cu, Zn, Ni and Cr) in the air for three consecutive months in an area where illegal e-waste recycling was in operation and compared the results with other two residential sites. In addition, we measured the concentrations of the same heavy metals in human blood to find out if there exists any correlation between environmental and biological exposure. Hypoxemia and hypertension were also determined for the comparison of health status amongst the study population. The study design comprised of three sites, which were selected on the basis of different major activities in the respective areas. Air samples were collected with the help of RDS and subjected to heavy metals analysis by ICP-OES, whereas blood samples were analyzed by ICP-MS. Results showed that amongst all study sites significant highest mean concentration of PM10 (243.310 ± 22.729 μg/m3) and its heavy metal was found at e-waste burning site (SIII). High levels of heavy metal in the air were responsible for the higher exposure to the residents of SIII. Therefore, the study concluded that e-waste burning by the informal sector has significantly contributed to the high levels of the air pollution, which in turn was responsible for the highest level of heavy metal exposure to the residents. This was also associated with the occurrence of cardiovascular morbidity namely hypertension amongst the inhabitants of SIII may indicate the effect of chronic exposure to the air pollution due to e-waste processing activities, which needs to be studied further.

Trace metals in e-waste lead to serious health risk through consumption of rice growing near an abandoned e-waste recycling site: Comparisons with PBDEs and AHFRs

Despite the endeavour to eradicate informal e-waste recycling, remediation of polluted sites is not mandatory in many developing countries and thus the hazard of pollutants remaining in soil is often overlooked. It is noteworthy that a majority of previous studies only analysed a few pollutants in e-waste to reflect the impact of informal e-waste recycling. However, the actual impact may have been largely underestimated since e-waste contains various groups of pollutants and the effect of some emerging pollutants in e-waste remains unexplored. Thus, this study examined the contamination of metals, PBDEs and AHFRs in the vicinity of an abandoned e-waste recycling site. The accumulation and translocation of these pollutants in rice plants cultivated at the nearby paddy field were measured to estimate the health risk through rice consumption. We revealed that the former e-waste burning site was still seriously contaminated with some metals (e.g. Sn, Sb and Ag, Igeo > 5), PBDEs (Igeo > 3) and AHFRs (Igeo > 3), which can disperse to the nearby paddy field and stream. The rice plants can effectively absorb some metals (e.g. Mo, Cr and Mn, BCF > 1), but not PBDEs and AHFRs (BCF < 0.15), from soil and translocate them to the leaves. Alarmingly, the health risk through rice consumption was high primarily due to Sb and Sn (HQ > 20), whereas PBDEs and AHFRs had limited contribution (HQ < 0.08). Our results imply that abandoned e-waste recycling sites still act as the pollution source, jeopardising the surrounding environment and human health. Since some trace metals (e.g. Sb and Sn) are seldom monitored, the impact of informal e-waste recycling would be more notorious than previously thought. Remediation work should be conducted promptly in abandoned e-waste recycling sites to protect the environment and human health.

Organophosphate flame retardants emitted from thermal treatment and open burning of e-waste.

Organophosphate flame retardants (OPFRs) have been increasingly produced and consumed since the gradual phase-out of polybrominated diphenyl ethers. Primitive recycling of e-waste can be a significant input source of OPFRs to the environment. Thermal treatment and open burning of typical e-wastes were conducted in a closed chamber to examine the emissions and the size distribution patterns of particle-bound OPFRs from these processes. The sum emission factors of OPFRs were 3.70 × 104-3.65 × 105 ng g-1 by thermal treatment and 5.22 × 103-9.27 × 104 ng g-1 by open burning. The output-input mass ratios of OPFRs for plastic casings were 0.030-116 and 0.012-7.1 by thermal treatment and open burning, respectively, and were 0.11-40 and 0.0014-6.7 for printed circuit boards. The size distribution patterns of OPFRs were characterized by one unimodal peak (0.56-1.0 μm) for thermal treatment and bimodal peaks (0.56-1.0 or 1.0-1.8 and 10-18 μm) for open burning. Particle-bound OPFRs appeared to form in affiliation with particles rather than by adsorption or deposition from the gaseous phase to particulate organic matter. With increasing amounts of OPFRs used in a variety of consumer products, the emissions of OPFRs to the environment are expected to increase continuously in the future.

A strong spatial association between e‐waste burn sites and childhood lymphoma in the West Bank, Palestine

A paper in the International Journal of Cancer analyzed Palestinian cancer registry data in the West Bank from 1998 to 2007, showing a cluster of elevated cancer incidence in rural villages in south-west Hebron, with a 4.10 risk ratio for childhood lymphoma (p = 0.0023). The paper called for investigation of the environmental or genetic etiologies of this cluster in an otherwise unremarkable rural area.1 Our research in these same villages shows them to be the center of an extensive informal electronic and electrical waste (e-waste) dismantling industry in Palestine, operating for almost two decades. This entails extensive open-burning of e-waste components to extract valuable metals or dispose of nonvaluable waste, releasing high concentrations of hazardous contaminants, which may be an important factor in the elevated cancer incidence. We offer a first step in assessing this link. We applied a novel multitemporal object-based method to map the prevalence and intensity of e-waste burn sites in the entire Hebron Governorate (1,060 km2 ) between 1999 and 2007. A weighted standard deviation ellipse of cumulative burn activity covers a smaller area (247 km2 ) very closely matching the childhood lymphoma cluster: it contains 85% of the core cluster area (RR of 4.1), and falls almost entirely (95%) within the broader area of elevated risk (RR of 2.8). Extensive international evidence linking informal e-waste processing to elevated cancer incidence and this strong spatial association of e-waste burning activity with a distinct unexplained cancer cluster in the Palestinian context signals the urgent need for investigation and intervention.

Characteristics of Polybrominated Diphenyl Ethers Released from Thermal Treatment and Open Burning of E-Waste.

Primitive processing of e-waste potentially releases abundant organic contaminants to the environment, but the magnitudes and mechanisms remain to be adequately addressed. We conducted thermal treatment and open burning of typical e-wastes, that is, plastics and printed circuit boards. Emission factors of the sum of 39 polybrominated diphenyl ethers (∑39PBDE) were 817-1.60 × 105 ng g-1 in thermal treatment and nondetected-9.14 × 104 ng g-1, in open burning. Airborne particles (87%) were the main carriers of PBDEs, followed by residual ashes (13%) and gaseous constituents (0.3%), in thermal treatment, while they were 30%, 43% and 27% in open burning. The output-input mass ratios of ∑39PBDE were 0.12-3.76 in thermal treatment and 0-0.16 in open burning. All PBDEs were largely affiliated with fine particles, with geometric mean diameters at 0.61-0.83 μm in thermal degradation and 0.57-1.16 μm in open burning from plastic casings, and 0.44-0.56 and nondetected- 0.55 μm, from printed circuit boards. Evaporation and reabsorption may be the main emission mechanisms for lightly brominated BDEs, but heavily brominated BDEs tend to affiliate with particles from heating or combustion. The different size distributions of particulate PBDEs in emission sources and adjacent air implicated a noteworthy redisposition process during atmospheric dispersal.