Developments in an industry-led R&D program for recycling PVC products in Japan

To facilitate recycling, not only R&D but also the creation of efficient recycling systems—collection and processing of recyclates as well as finding appropriate end-uses—is essentially important. PVC has a particular advantage in regards to mechanical recycling when compared to other major plastics. However, there is no one-size-fits-all approach to a solution. Specific situations of used or off-cut products and their applications need to be well studied. Vinyl industry in Japan has devoted itself for many years to the promotion of recycling of vinyl products. It started an R&D support program in 2007 and seven projects have been completed since then. Some of the new developments include mechanical recycling for products like wall covering and tarpaulin which were considered difficult to recycle in the past. Progress in chemical recycling has been made with a technology for the removal of chlorine from shredder dusts. Recovery of chlorine is a challenge for the future. Collaboration among the various players involved in the recycling of a specific product is essential for obtaining a successful result.     

Feedstock recycling of waste polymeric material

The first International Symposium on Feedstock Recycling of Polymeric Materials (ISFR) was hosted in 1999 in Sendai, Japan. Since then, the ISFR has been held five times in different places in Asia and Europe. Each of these conferences focused on special issues covered by the Journal of Material Cycles and Waste Management. The topics included thermal processes with and without catalysts, wet processes in various solvents, the dehydrochlorination of PVC, mechanical recycling and separation techniques, as well as the treatment of biomaterials. This review is a compilation of the most interesting and important developments discussed at the ISFR during the last decade.     

An estimation of the social costs of landfill siting using a choice experiment

This paper examines public preferences on siting landfills using a choice experiment. A choice experiment is a method that elicits public preferences directly through questionnaires. This paper focuses on possible negative effects of a hypothetical landfill siting on residents who are assumed to live around the landfill. The results of this analysis clearly show that the residents evaluate accepting waste originating from outside their community quite negatively, especially industrial waste originating from the Tokyo Metropolitan Area. Large external costs also are seen for siting landfills near areas that are sources of drinking water. In addition, the results show that the NIMBY syndrome of the residents weakens as the hypothetical landfill site is farther away. Considering three hypothetical siting plans, external costs based on public preferences are estimated. The social costs, which are the sum of the private costs and external costs, are then calculated. The results of the case study indicate that the option with the lowest private cost it is not always the option with the lowest social cost.     

Autotrophic denitrification for nitrate and nitrite removal using sulfur-limestone

In the study, both nitrate and nitrite could be removed effectively using sulfur-limestone, and the bacteria involved in sulfur-based denitrification for nitrate and nitrite removal were of the same species.     

Alkaline hydrolysis of photovoltaic backsheet containing PET and PVDF for the recycling of PVDF

Recovering fluorine from end-of-life products is crucial for the sustainable production and consumption of fluorine-containing compounds because fluorspar, an important natural resource for fluorine, is currently at a supply risk. In this study, we investigated the feasibility of chemically recycling a fluorine-containing photovoltaic (PV) backsheet for fluoropolymer recycling. Herein, a PV backsheet consisting of laminated polyethylene terephthalate (PET) and polyvinylidene fluoride (PVDF) was treated with different concentrations of sodium hydroxide (NaOH) to hydrolyze the PET layer to water-soluble sodium terephthalate (Na₂TP) and to separate pure PVDF layer as a solid material. Optimized alkaline conditions (up to 10 M NaOH at 100 °C for 2 h) were determined, under which 87% of the PET layer could be decomposed without any significant deterioration of the PVDF layer. The hydrolysis kinetics of PET layer in NaOH could be explained by the modified shrinking-core model. Considering that the mass of end-of-life PV panels in Japan is estimated to increase to approximately 280,000 tons per year by 2036, PV backsheets are attractive candidates for fluoropolymer recycling, which can be effectively achieved using chemical recycling approach demonstrated in this study.

     

Removal of chloride from ethylene glycol solution using alumina/zeolite membrane as a physical boundary between the organic and aqueous phases

The permeation of Cl^? ions from a NaCl/ethylene glycol (EG) solution during electrodialysis was investigated using alumina and alumina/zeolite membranes. Voltage changes had very little effect on Cl^? permeation through the alumina membrane, suggesting that the driving force for the permeation was concentration-gradient-induced diffusion, and not the electric field. Solvation of the Na⁺ ions by EG resulted in EG migration through the membrane. Replacement of the deionized water (electrolyte) in the anodic cell with NaOH resulted in increased Cl^? permeation, although a greater amount of EG migrated into the NaOH solution as well. No notable difference was observed in Cl^? permeation through the alumina and alumina/zeolite membranes, but EG migration decreased when using the latter membrane, suggesting that EG migration was prevented by the zeolite layer. The proposed alumina/zeolite membrane is, hence, useful for solvent recovery by electrodialysis, but its mechanical stability must be improved for industrial applications.     

Distribution and binding pattern of benzo(a)pyrene in rat liver,lung and kidney constituents after oral administration

Orally administered ³H‐benzo(a)pyrene (BP) was persistent in protein fraction of liver, lung and kidney. The radioactivity in this fraction increased with time after administration and accounted for about 50%, 40% and 65% of total radioactivity in liver, lung and kidney, respectively at 48 hr. The BP metabolites binding proteins were located in cytosol and had molecular weights of 40,000–60,000 and 80,000–100,000 as determined by gel filtration and polyacrylamide gel disc electrophoresis. In addition, at 48hr after administration, about 80% of radioactivity in high molecular weight protein fraction was found to be precipitated by trichloroacetic acid treatment.

These results suggest that BP metabolites might be transported by and are persistent in these protein fractions of liver, lung and kidney if the intake of BP is continuous. These proteins, therefore, appeared to be closely related to cell toxicity or mutagenicity in these organs as well as DNA.     

Validation of diffusive mini-samplers for aldehyde and VOC and its feasibility for measuring the exposure levels of elementary school children

Exposure to various chemicals can cause adverse effects to health, such as asthma and allergies, especially in children. Data on personal exposure levels in children are scarce, thus small lightweight diffusive mini-samplers for aldehydes and volatile organic compounds (VOCs) were designed to measure the exposure level of children to these chemicals. The aim of the study was to validate and examine the applicability of these mini-samplers for measuring daily chemical exposure. The diffusive mini-samplers are 20 mm in length, 11 mm in diameter, and 1.67 g in weight. The devices are cylindrically shaped with polytetrafluoroethylene membrane filters placed at each end. To measure aldehydes and acetone, 20 mg of 2,4-dinitrophenylhydrazine was used as an absorbent. To measure VOCs, a carbon molecular sieve was used. The sampling rate for each chemical was determined by parallel sampling with active samplers in a closed exposure bag. The blank levels of the chemicals and the storage stability of the device were tested. The mini-samplers were compared to commercially available diffusive samplers. To examine the applicability of the samplers, 65 elementary school children carried them for 24 h. The sampling rates for formaldehyde, acetaldehyde, and acetone were 20.9, 22.9, and 19.7 mL min(-1), respectively. The limits of quantification (LOQ) for the 24-hour sampling by high-performance liquid chromatography/ultraviolet (HPLC/UV) analysis were 8.3, 7.6, and 8.8 μg m(-3) for formaldehyde, acetaldehyde, and acetone, respectively. The sampling rates for the 11 VOCs were determined and ranged from 3.3 mL min(-1) for styrene and 2-ethyl-1-hexanol to 11.7 mL min(-1) for benzene. The LOQ for the 24-hour sampling by gas chromatography-mass spectrometry (GC-MS) analysis ranged from 5.9-105.2 μg m(-3), 1.1-24.7 parts per billion. The storage stability after 5 days ranged from 94.8 to 118.2%. Formaldehyde, acetone, benzene, and toluene were detected above the LOQ in more than 90% of the children, and the median concentrations were 21.7, 20.9, 10.1, and 21.5 μg m(-3), respectively. This study shows that the diffusive samplers developed were suitable for children to carry and were capable of measuring the children's daily chemical exposure.     

Applications of a hydro-biogeochemical model and long-term simulations of the effects of logging in forested watersheds

We simulated hydrological and biogeochemical responses to logging in a forested watershed to determine the vulnerability and/or resiliency of the forest ecosystems in the Lake Shumarinai Basin in northern Hokkaido, Japan. We used a biogeochemical model (PnET-CN) and a rainfall–runoff model (HYCYMODEL) to predict ecosystem responses. The PnET-CN model simulated well the observed NO₃ ⁻ concentrations in streamwater, particularly at high concentrations during snowmelt; however, the model could not simulate small increases in NO₃ ⁻ during the summer. By considering hydrological processes within the watershed and combining the model with the HYCYMODEL (PnET + HYCYMODEL), the seasonality of streamwater NO₃ ⁻ concentrations was better simulated. Using these models, the long-term effects of logging were simulated for coniferous, deciduous, and mixed forests. NO₃ ⁻ concentrations in streamwater increased in response to the logging disturbance in both coniferous and deciduous forests. In the coniferous forest, NO₃ ⁻ concentrations reached a maximum 10 years after logging, and high concentrations persisted for 30 years. In contrast, NO₃ ⁻ concentrations in the deciduous forest reached a maximum within 3–4 years and recovered to pre-disturbance levels after 15 years. We also used the models to determine the effects of different sizes and types (coniferous, deciduous, and mixed forest) of logging areas on Lake Shumarinai. The model results indicated that large areas of cutting require more than 100 years for complete lake recovery. Whereas the annual discharge to the lake minimally increased, the annual NO₃ ⁻ load greatly increased. Our simulation results elucidate the vulnerability and resiliency of forest ecosystems and provide valuable information for ecosystem management.