Time bomb or hidden treasure? Characteristics of junk TVs and of the US households who store them

Within the growing stockpile of electronic waste (e-waste), TVs are especially of concern in the US because of their number (which is known imprecisely), their low recycling rate, and their material content: cathode ray tube televisions contain lead, and both rear projection and flat panel displays contain mercury, in addition to other potentially toxic materials. Based on a unique dataset from a 2010 survey, our count models show that pro-environmental behavior, age, education, household size, marital status, gender of the head of household, dwelling type, and geographic location are statistically significant variables for explaining the number of broken or obsolete (junk) TVs stored by US households. We also estimate that they are storing approximately 84.1 million junk TVs, which represents 40 pounds of scrap per household. Materials in each of these junk TVs are worth $21 on average at January 2012 materials prices, which sets an upper bound on collecting and recycling costs. This information should be helpful for developing more effective recycling strategies for TVs in the e-waste stream.     

California households' willingness to pay for ‘green’ electronics

Concerns about rapid increases in the volume of electronic waste (e-waste) and its potential toxicity have sharpened policy makers' interest for extended producer responsibility to encourage manufacturers of consumer electronic devices (CEDs) to ‘design for the environment’. This paper examines consumer willingness to pay for ‘green’ electronics based on a 2004 mail survey of California households. Using ordered logit models, it was found that significant predictors of willingness to pay for ‘greener’ computers and cell phones include age, income, education, beliefs about the role of government for improving environmental quality, as well as environmental attitudes and behaviors, but neither gender nor political affiliation. Although most respondents are willing to pay only a 1% premium for ‘greener’ CEDs, innovation and EU directives may soon make them competitive with conventional CEDs.     

Large-scale aircraft observations of ultra-fine and fine particle concentrations in the remote Siberian troposphere: New particle formation studies

Ultra-fine particle number concentrations were measured over Siberia during two large-scale airborne measurement campaigns in April and September 2006. During both campaigns, an aircraft flew between Novosibirsk and Yakutsk, collecting every 200 km vertical profiles up to 7 km. This dataset was completed by 5 years of monthly profiles above Novosibirsk. Particle number concentration was measured in the size ranges 3–70 and 70–200 nm, along with other tracers. Free troposphere (FT) particle concentrations (N_3–200) varied between 60 and 460 cm^?3, inferior to boundary layer concentrations (100–7000 cm^?3). In April, high concentrations of ～500 cm^?3 were observed in a polluted air mass recently uplifted at 5–6 km altitude over eastern Siberia, with no sign of significant new particle formation. In September, particle concentrations decreased with altitude, but with a steeper gradient in N_70–200 compared to N_3–70, the latter accounting for 90% of the total particle concentration in the free troposphere at 6–7 km altitude. Because ultra-fine particles presumably have short lifetimes, these observed particles could have been formed in situ in the clean Siberian atmosphere. Two cases of possible nucleation with high concentration and N_3–70/N_70–200 ratios are reported for the September campaign, in the upper troposphere and in cloud outflow in the mid-troposphere. In the seasonal analysis, a FT N_3–70 maximum is found in July–August between 6 and 7 km altitude, with N_3–70 accounting for ～90% of N_3–200 supporting the hypothesis of in situ formation in the FT. A secondary FT maximum of N_3–70 was identified later in autumn. In the boundary layer, seasonally maximum N_3–70 concentrations were found over Novosibirsk in May and September, but not in summer, possibly due to scavenging by precipitations and a large condensational sink from biomass burning aerosols. Our dataset has a limited size resolution and no speciation capability; more investigation is thus required to understand the conditions leading to in situ nucleation processes in the Siberian air shed.     

Stability considerations of aspartame in the direct analysis of artificial sweeteners in water samples using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)

A HPLC-MS/MS method is presented for the simultaneous determination of frequently used artificial sweeteners (ASs) and the main metabolite of aspartame (ASP), diketopiperazine (DKP), in environmental water samples using the direct-injection (DI) technique, thereby achieving limits of quantification (LOQ) of 10 ng L⁻¹. For a reliable quantification of ASP pH should be adjusted to 4.3 to prevent formation of the metabolite. Acesulfame (ACE), saccharin (SAC), cyclamate (CYC) and sucralose (SUC) were ubiquitously found in water samples. Highest concentrations up to 61 μg L⁻¹ of ACE were found in wastewater effluents, followed by surface water with concentrations up to 7 μg L⁻¹, lakes up to 600 ng L⁻¹ and groundwater and tap water up to 70 ng L⁻¹. The metabolite DKP was only detected in wastewater up to 200 ng L⁻¹ and at low detection frequencies.     

How much e-waste is there in US basements and attics? Results from a national survey

The fate of used electronic products (e-waste) is of increasing concern because of their toxicity and the growing volume of e-waste. Addressing these concerns requires developing the recycling infrastructure, but good estimates of the volume of e-waste stored by US households are still unavailable. In this context, we make two contributions based on a national random survey of 2136 US households. First, we explain how much e-waste is stored by US households using count models. Significant explanatory variables include age, marital and employment status, ethnicity, household size, previous e-waste recycling behavior, and to some extent education, home ownership, and understanding the consequences of recycling, but neither income nor knowledge of e-waste recycling laws. Second, we estimate that on average, each US household has 4.1 small (≤10 pounds) and 2.4 large e-waste items in storage. Although these numbers are likely lower bounds, they are higher than recent US Environmental Protection Agency (EPA) estimates (based on narrower product categories). This suggests that the backlog of e-waste in the US is likely larger than generally believed; it calls for developing the recycling infrastructure but also for targeted recycling campaigns.     

Financing electronic waste recycling Californian households' willingness to pay advanced recycling fees

The growth of electronic waste (e-waste) is of increasing concern because of its toxic content and low recycling rates. The e-waste recycling infrastructure needs to be developed, yet little is known about people's willingness to fund its expansion. This paper examines this issue based on a 2004 mail survey of California households. Using an ordered logit model, we find that age, income, beliefs about government and business roles, proximity to existing recycling facilities, community density, education, and environmental attitudes are significant factors for explaining people's willingness to pay an advanced recycling fee (ARF) for electronics. Most respondents are willing to support a 1% ARF. Our results suggest that policymakers should target middle-aged and older adults, improve programs in communities with existing recycling centers or in rural communities, and consider public-private partnerships for e-waste recycling programs.     

Comparing solid phase extraction and direct injection for the analysis of ultra-trace levels of relevant explosives in lake water and tributaries using liquid chromatography-electrospray tandem mass spectrometry

Off-line solid phase extraction and direct injection analysis were evaluated for the determination of traces of explosives such as TNT and its mono and diamino metabolites, HMX, RDX, nitroglycerin and PETN in lake water and tributaries applying liquid chromatography-electrospray tandem mass spectrometry. Improved chromatographic separation was achieved on a phenyl based stationary phase with baseline resolution of the mono- and diamino metabolites of TNT. Identification and quantification of the target compounds was performed by multiple reaction monitoring applying electrospray ionization in either the positive mode for the diaminometabolites of TNT or the negative mode for all other compounds. An extensive method validation was performed and limits of quantification were obtained for the explosives in preconcentrated lake water samples from 0.03 to 1 ng l(-1) and 0.1 to 5 ng l(-1) in river water. Direct injection analysis revealed comparable results to preconcentrated water samples for the most persistent explosives. Analysis of lake water samples collected at different depths showed the presence of HMX, RDX and PETN at concentrations from 0.1 to 0.4 ng l(-1). The analysis of main tributaries revealed concentrations from 0.1 to 0.9 ng l(-1) of the same compounds. They seem to be responsible for the contamination of the explosives in the lakes.