Cellulose acetate (CA) is one of widely used polymers for chemical and medical applications due to its versatile physico-chemical functionalities. Although its recycle is available after a deacetylation process, the recycle process releases a huge amount of wastewater. Thus, this study investigated a direct disposal process of CA with its valorization to syngas (H₂ and CO) through pyrolysis. To construct more environmentally benign process, CO₂ was used as a co-feedstock with CA to simultaneously convert them into syngas. Pyrolysis of CA in N₂ was performed as a reference study to examine the effectiveness of CO₂ on valorization of CA. Acetic acid and methyl acetate were main volatile pyrolysates (VPs) from CA pyrolysis, and the further thermal cracking of VPs resulted in syngas and CH₄ formations under both N₂ and CO₂ conditions. To expedite syngas formations, multi-stage pyrolysis (two-stage pyrolysis) and catalytic pyrolysis were employed. With the increased thermal energy through two-stage pyrolysis, four times more production of syngas was shown, comparing to the result of a single-stage pyrolysis. With Ni catalysts, the syngas formation was the two orders of magnitude higher than the single-stage pyrolysis, and the significant enhancement of CO formation was shown in the presence of CO₂ due to combined effects of CO₂ and the Ni-based catalysts. This CO enhancement resulted from catalytically expedited gas phase reactions between CO₂ and VPs evolved from CA. In addition, the CO₂ contributed to the suppression of coke deposition on the catalyst, thereby suggesting more technical and environmental benefits of CO₂ as a reactive co-feedstock of pyrolysis in reference to N₂. Therefore, this study proved the direct and versatile technical platform to convert CA and CO₂ into syngas.

Coupling with triolein-embedded cellulose acetate membrane (TECAM) technique, hydroxypropyl β-cyclodextrins (HPCD) extraction method, and the greenhouse pot experiments, the influences of biochars on polychlorinated biphenyls (PCBs) bioavailability in soil to plant (Brassica chinensis L. and Daucus carota) were investigated. Addition of 2% biochars to soils significantly reduced the uptake of PCBs in plant, especially for di-, tri- and tetra-chlorobiphenyls. PCBs concentrations in the roots of B. chinensis and D. carota were reduced for 61.5–93.7%, and 12.7–62.4%, respectively in the presence of biochars. The kinetic study showed that in the soils amended with/without biochars, PCBs concentrations accumulated in TECAM, as well as in the HPCD extraction solution, followed significant linear relationships with those in plant roots. Application of biochars to soil is a potentially promising method to reduce PCBs bioavailability whereas TECAM technique can be a useful tool to predict the bioavailability of PCBs in soil.

Triolein embedded cellulose acetate membrane (TECAM) was used for passive sampling of the fraction of naphthalene, phenanthrene, pyrene and benzo[a]pyrene in 18 field-contaminated soils. The sampling process of PAHs by TECAM fitted well with a first-order kinetics model and PAHs reached 95% of equilibrium in TECAM within 20 h. Concentrations of PAHs in TECAM (CTECAM) correlated well with the concentrations in soils (r2 = 0.693-0.962, p < 0.001). Furthermore, concentrations of PAHs determined in the soil solution were very close to the values estimated by CTECAM and the partition coefficient between TECAM and water (KTECAM-w). After lipid normalization nearly 1:1 relationships were observed between PAH concentrations in TECAMs and earthworms exposed to the soils (r2 = 0.591–0.824, n = 18, p < 0.01). These results suggest that TECAM can be a useful tool to predict bioavailability of PAHs in field-contaminated soils.

Smoked cigarette filters a. k.a. “butts”, composed of plastic (e.g. cellulose acetate) are one of the world’s most common litter items. In response to concerns about plastic pollution, biodegradable cellulose filters are being promoted as an environmentally safe alternative, however, once smoked, both contain toxins which can leach once discarded. The impacts of biodegradable butts as littered items on the receiving environment, in comparison with conventional butts has not yet been assessed. A freshwater mesocosm experiment was used to test the effects of leachate from smoked cellulose acetate versus smoked cellulose filters at a range of concentrations (0, 0.2, 1 and 5 butts L⁻¹) on the mortality and behaviour of four freshwater invertebrates (Dreissena polymorpha, Polycelis nigra, Planorbis planorbis and Bithynia tentaculata). Leachate derived from 5 butts L⁻¹ of either type of filter caused 60–100% mortality to all species within 5 days. Leachate derived from 1 butt L⁻¹ of either type resulted in adults being less active than those exposed to no or 0.2 butts L⁻¹ leachate. Cigarette butts, therefore, regardless of their perceived degradability can cause mortality and decreased activity of key freshwater invertebrates and should always be disposed of responsibly.

Organic pollutants in the Arctic seas have been of concern to many researchers; however, the vast dynamic marine water poses challenges to their comprehensive monitoring within appropriate spatial and temporal scales in the Arctic. In this study, on-board passive sampling of organic pollutants using a self-developed device coupled with triolein-embedded cellulose acetate membranes (TECAMs) was performed during an Arctic cruise. The TECAM extracts were used for target analysis of organophosphorus flame retardants (PFRs), and non-target screening of persistent, bioaccumulative, and toxic (PBT) contaminants using two-dimensional gas chromatography with time-of-flight mass spectrometry (GC × GC-TOFMS). Sixteen chemicals were screened out as PBT contaminants from the 1500 features in the non-target analysis and further identified. Consequently, two chlorinated PFRs (tris(chloroisopropyl)phosphate and tris(1,3-dichloroisopropyl)phosphate) and four PBT contaminants (4-tert-butylphenol, 2-isopropylnaphthalene, 1,1,3-trimethyl-3-phenylindane, and 1-phenylnonan-1-one) were accurately quantified, with the temporally and spatially integrated concentrations ranging from 0.83 ng L⁻¹ to 20.82 ng L⁻¹ in the seawaters. Sources and transport of the contaminants were studied, and ocean current transport (West Spitsbergen Current, WSC) and local sources (human settlement, Arctic oil exploitation, and petroleum fuel emissions) were found to contribute to the presence of the different contaminants. Finally, annual transport fluxes of the contaminants from the North Atlantic to the Arctic Ocean by WSC were estimated, and the results indicate that their hazard to the Arctic should be concerned.

Plastic in the environment is considered an emerging pollutant of global concern. In spite of intensive research, many questions remain open, such as the processes that drive the deposition and remobilization of plastic debris on river beaches. The objectives of this study were: i) to analyze the influence of the natural hydrological fluctuations and wind intensity on the distribution of mesoplastic (0.5–2.5 cm) and macroplastic (>2.5 cm) debris in beach sediments of a large river, ii) to describe the type of plastic debris found and iii) to explore potential relations between the number of items and weight of macro- and mesoplastics. Our results suggest that, during lowering water levels, flow removes the plastic debris and transports it further downstream. Conversely, when the beach sediments remain exposed during long periods, the plastic debris accumulates considerably. Nevertheless, the influence of wind intensity on plastic debris transport was comparatively negligible. In other words, in our study the water flow had a greater capacity to remobilize and transport plastic debris than the wind. The most abundant mesoplastic items were foam, hard plastic, film and small fragments of fishing line. The dominant macroplastic items recorded were pieces of fishing line (nylon) and cigarette filters (cellulose acetate), typically discarded by beach users. Other items found in large quantities were soft packaging elements (expanded polystyrene), hard plastic containers (polystyrene, polyethylene terephthalate) and beverage bottles (polyethylene terephthalate), typical items of domestic use in the Paraná River region. Finally, we found that the density of macroplastic items is highly correlated to the density of mesoplastic items, serving as surrogate for further estimations. Our results could help to develop better mitigation strategies in seasonal riverscapes, based on the influence of the hydrological cycle and the characteristics of the most abundant meso- and macroplastics.

Triolein embedded cellulose acetate membrane (TECAM) passive samplers provide potentially powerful tool for monitoring time weighted average concentrations (CTWA) of trace hydrophobic organic contaminants in water. To study the field performance of TECAM, exchange kinetics of chemicals between water and TECAM were studied at different temperature and water flow rates. Results showed that the uptake rate constant (kᵤ) in TECAM was less sensitive to temperature variation than the SPMD and Chemcatcher. The kᵤ in TECAM was sensitive to even a slight change of the flow rate, which required the field calibration using performance reference compounds (PRCs). To estimate CTWA by TECAM, both empirical model and WBL model were compared in laboratory conditions, and only small differences were observed between the predicted and measured kᵤ. Field validation was conducted to test the sampler performance alongside spot sampling. A good agreement of water concentration was obtained by the two sampling techniques.

Microplastics are small plastic particles found ubiquitously in marine environments. In this study, a hybridized method was developed for the extraction of microplastics (45–1000 μm) from sediments using sodium bromide solution for density separation. Method development was tested using spiked microplastics as internal standards. The method was then used to extract microplastics from sediments in Narragansett Bay, Rhode Island, USA. Suspect microplastics were analyzed with Raman spectroscopy. Microplastic abundance ranged from 40 particles/100 g sediment to 4.6 million particles/100 g sediment (wet weight). Cellulose acetate fibers were the most abundant microplastic. These results are some of the first data for microplastics in Rhode Island sediments.

Outdoor mesocosms with constantly flowing natural seawater were used to test the effects of littered cigarette butts on the filter feeder Mytilus edulis (blue mussel), the macroalga, Ulva lactuca (sea lettuce) and sediment microphytobenthos in a semi-natural marine setting. Either conventional, cellulose acetate, or biodegradable, cellulose, smoked cigarette butts were added at densities of 0.25 or 1 butt L⁻¹. The clearance rates of mussels exposed to 1 butt L⁻¹ of cellulose acetate butts were three times less than the controls. The growth of U. lactuca was not measurably affected by cigarette butts, however the sediment chlorophyll content was significantly less in mesocosms exposed to 0.25 and 1 butt L⁻¹ of cellulose acetate butts. These effects occurred despite constant replacement of seawater indicating how hazardous conventional cigarette butts are to marine life. Biodegradable cellulose cigarette butts had minimal effects on the measured variables but should still not be discarded as litter.

This paper increases knowledge on litter transfer from sediments towards the trophic web throughout sea cucumbers, key protected benthic species. In October, sediment and holothurian samples from seventeen sampling sites from Croatian Islands characterized by different levels of protection (Silba n = 7; Telašćica MPA n = 10) were collected. Collected particles ranged in sediments within 113.4–377.8 items/kg d.w., and in holothurians within 0.6–9.4 items/animal, showing sizes within 1.4–10,493 μm. In holothurians, cellulose and cellulose acetate (non-synthetic materials) mean percentages were within 5.0–12.7% of the total amount of particles. Nylon fibres ranged within 0–26.7%; while PP, PE, PA, and PS% were more abundant than in sediments. Among factors of variability tested, “island group” and “level of protection” resulted to affect plastic composition in sediments. Otherwise, other environmental factors (i.e. orientation, morphology of sampling site, P. oceanica) were significantly related to chemical composition of microplastic ingested by holothurians.