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Marine vertebrates, particularly green sea turtles, are especially vulnerable to plastic pollution through ingestion or entanglement. This study investigated wild juvenile green sea turtles (Chelonia mydas) from two Ecuadorian national parks (Galápagos and Machallilla) to assess the prevalence of plastic pollution in their feces and its potential impact on various health metrics. We analyzed fecal samples from 46 juvenile green sea turtles using Fourier transform infrared spectroscopy (FT-IR) to quantify microplastics (MPs). A complementary methodology using pressurized liquid extraction with double-shot pyrolysis-mass spectrometry gas chromatography (Pyr-GC/MS) was also employed to quantify synthetic polymer mass concentrations. The results from these analyses were compared with blood analytes. FT-IR analysis revealed a mean of 4.4±5.2 MPs/g in fecal samples, with the highest quantities found in the Galápagos Marine Reserve (GMR). The most common MPs shape identified were fibers (x̄= 3.8±4.5 MPs/g), and the predominant synthetic polymers were polyvinyl alcohol (PVOH) and polyacrylates (PMMA). The daily intake of MPs by the sampled turtles ranged from a minimum of 312±409 MPs/day to a maximum of 430±563 MPs/day. Pyr-GC/MS analysis detected polyethylene (PE) with a mean of 367±1158 µg/g and polypropylene (PP) with a mean of 155±434 µg/g in fecal samples, with the highest pollution levels observed in the GMR. Both FT-IR and Pyr-GC/MS techniques detected plastic pollution in 98% of the sampled population. Although both FT-IR and Pyr-GC/MS are reliable methods, they produced slightly different results due to methodological variations. However, both supported the finding that turtles in the GMR were exposed to higher rates of plastic ingestion. Despite the turtles appearing clinically healthy based on blood analysis, significant differences in eleven health metrics were observed between turtles classified as less at risk and those most at risk for plastic pollution. Further research is necessary to understand the potential health implications of these findings.

Microplastic (MP) contamination has become a problem of great interest to the community at large. The detection of these particles in different ecosystems and foods has been the subject of study. However, the focus of these investigations has been on the identification and quantification of PM by DSC and Pyr-GC/MS and not on how they are transported to reach the air we breathe. In this study, the values of morphological parameters for plastic particles in a range between 1 and 2000 µm, present in the breathable air of 20 neighborhoods in the city of Cartagena, Colombia, were obtained to determine the characteristics that make these particles airborne. The values of parameters were obtained, such as roundness, sphericity, curvature, and the convexity of the particle, as well as its compactness and size, which influence its transport through the air and its ability to be ingested and inhaled. The data obtained in this study allows for simulations and the analysis of the behavior of microplastics once in the environment to predict future settlements. The DSC showed us the melting temperatures of PP, PE, PET, and PS, the Pyr-GC/MS showed the fragmentation patterns, and the presence of these MPs in the samples was confirmed. [ABSTRACT FROM AUTHOR]

Pyrolysis-GC/MS is increasingly used to quantify microplastics (MP) in environmental samples. In general, prior to analysis, purification steps are carried out to reduce the environmental matrix in sediment samples. The conventionally used protocol of density separation followed by digestion of organic matter does not allow for complete isolation of MP from the associated organic and mineral matter. Among the pyrolysis products used as indicator compounds for plastic polymers, some may originate from other substances present in the environmental samples. In this paper, the indicator compounds are reviewed for the most common polymers: PE, PP, PS, PET and PVC and selected taking into account potential interactions with substances present in environmental matrices. Even after a purification step, a residual mineral fraction remains in a sediment sample, including matrix effects. This effect may be positive or negative, depending on the investigated polymer and is thus important to consider when using Pyr-GC/MS for the quantification of MP in sediment samples. It also shows that no external calibration can be used to reliably quantify MP in such samples and that the use of internal standards is compulsory. [ABSTRACT FROM AUTHOR]

Microplastic (MP) contamination has become a problem of great interest to the community at large. The detection of these particles in different ecosystems and foods has been the subject of study. However, the focus of these investigations has been on the identification and quantification of PM by DSC and Pyr-GC/MS and not on how they are transported to reach the air we breathe. In this study, the values of morphological parameters for plastic particles in a range between 1 and 2000 µm, present in the breathable air of 20 neighborhoods in the city of Cartagena, Colombia, were obtained to determine the characteristics that make these particles airborne. The values of parameters were obtained, such as roundness, sphericity, curvature, and the convexity of the particle, as well as its compactness and size, which influence its transport through the air and its ability to be ingested and inhaled. The data obtained in this study allows for simulations and the analysis of the behavior of microplastics once in the environment to predict future settlements. The DSC showed us the melting temperatures of PP, PE, PET, and PS, the Pyr-GC/MS showed the fragmentation patterns, and the presence of these MPs in the samples was confirmed.

Sampling, separation, detection, and characterization of microplastics (MPs) dispersed in natural water bodies and ecosystems is a challenging and critical issue for a better understanding of the hazards for the environment posed by such nearly ubiquitous and still largely unknown form of pollution. There is still the need for exhaustive, reliable, accurate, reasonably fast, and cost-efficient analytical protocols allowing the quantification not only of MPs but also of nanoplastics (NPs) and of the harmful molecular pollutants that may result from degrading plastics. Here a set of newly developed analytical protocols, integrated with specialized techniques such as pyrolysis-gas chromatography-mass spectrometry (Py-GC/MS), for the accurate and selective determination of the polymers most commonly found as MPs polluting marine and freshwater sediments are presented. In addition, the results of an investigation on the low molecular weight volatile organic compounds (VOCs) released upon photo-oxidative degradation of microplastics highlight the important role of photoinduced fragmentation at a molecular level both as a potential source of hazardous chemicals and as accelerators of the overall degradation of floating or stranded plastic debris. [ABSTRACT FROM AUTHOR]

• Mass concentration of nanoplastics investigated across different treatment stages of WWTPs by Pyr-GC/MS. • Eight different nanoplastics (PMMA, nylon 6, nylon 66, PC, PS, PET, PP, PE) identified and quantified. • Nylon 66, PE, PP, PET, and nylon 6 were the most prevalent nanoplastics types detected in the wastewater samples. • Up to 96 % of the nanoplastics identified were removed from effluent during treatment. Municipal wastewater treatment plants (WWTPs) play a crucial role in the collection and redistribution of plastic particles from both households and industries, contributing to their presence in the environment. Previous studies investigating the levels of plastics in WWTPs, and their removal rates have primarily focused on polymer type, size, shape, colour, and particle count, while comprehensive understanding of the mass concentration of plastic particles, particularly those <1 µm (nanoplastics), remains unclear and lacking. In this study, pyrolysis gas chromatography–mass spectrometry was used to simultaneously determine the mass concentration of nine selected polymers (i.e., polyethylene (PE), polypropylene (PP), polystyrene (PS), poly(ethylene terephthalate) (PET), nylon 6, nylon 66, polyvinylchloride (PVC), poly(methyl methacrylate) (PMMA) and polycarbonate (PC)) below 1 µm in size across the treatment processes or stages of three WWTPs in Australia. All the targeted nanoplastics were detected at concentrations between 0.04 and 7.3 µg/L. Nylon 66 (0.2–7.3 µg/L), PE (0.1–6.6 µg/L), PP (0.1–4.5 µg/L), Nylon 6 (0.1–3.6 µg/L) and PET (0.1–2.2 µg/L), were the predominant polymers in the samples. The mass concentration of the total nanoplastics decreased from 27.7, 18 and 9.1 µg/L in the influent to 1, 1.4 and 0.8 µg/L in the effluent, with approximate removal rates of 96 %, 92 % and 91 % in plants A, B and C, respectively. Based on annual wastewater effluent discharge, it is estimated that approximately 24, 2 and 0.7 kg of nanoplastics are released into the environment per year for WWTPs A, B and C, respectively. This study investigated the mass concentrations and removal rates of nanoplastics with a size range of 0.01–1 µm in wastewater, providing important insight into the pollution levels and distribution patterns of nanoplastics in Australian WWTPs. [Display omitted] [ABSTRACT FROM AUTHOR]

Valorizing rice straw could mitigate the detrimental health and environmental consequences of disposal through field burning. An essential step for achieving this is reducing straw recalcitrance to digestion by either enzymes or animals to facilitate uses as fertilizer, animal feed, or conversion into fuels and chemicals. In the present work, we developed and characterized a Philippine rice diversity panel to explore the chemical basis of biomass recalcitrance. We used high throughput phenotyping of straw samples from the panel to identify chemical compounds that confer recalcitrance. We determined the saccharification potential, silica, ferulic, and p-coumaric acid content in each rice accession, as well as the chemical fingerprint of biomass composition using pyrolysis followed by GC/MS. Multivariate analysis of the phenotypic data allowed us to characterize the relationship between biomass components and straw saccharification establishing that Si, ferulic acid and coumaric acid are inversely correlated with saccharification. PCA analysis showed that pyrolysis products derived from lignin constitute the largest proportion of compounds inversely correlated with saccharification. • A rice association panel was characterized for straw quality. • Pyr-GC/MS fingerprinting of straw shows the compositional diversity in the panel. • Silica, coumaric acid and ferulic acid are inversely correlated to saccharification. • We identified pyrolysis peaks associated with saccharification potential. [ABSTRACT FROM AUTHOR]

Nanoplastics are emerging environmental contaminants, but their presence in environmental and potable water remains largely understudied due to the absence of quantitative analytical methods. In this study, we developed and validated a pretreatment method that combines hydrogen peroxide digestion and Amicon® Stirred Cell ultrafiltration (at 100 kDa, approximately 10 nm) with subsequent detection by pyrolysis gas chromatography–mass spectrometry (Pyr-GC/MS). This method allows for the simultaneous identification and quantification of nine selected nanoplastic types, including poly(ethylene terephthalate) (PET), polyethylene (PE), polycarbonate (PC), polypropylene (PP), poly(methyl methacrylate) (PMMA), polystyrene (PS), polyvinylchloride (PVC), nylon 6, and nylon 66, in environmental and potable water samples based on polymer-specific mass concentration. Limits of quantification ranged from 0.01 to 0.44 µg/L, demonstrating the method's ability to quantitatively detect nanoplastics in environmental and potable water samples. Most of the selected nanoplastics were detected at concentrations of between 0.04 and 1.17 µg/L, except for PC, which was consistently below the limit of detection (<0.44 µg/L). The prevalent polymer components in the samples were PE (0.10 – 1.17 µg/L), PET (0.06 – 0.91 µg/L), PP (0.04 – 0.79 µg/L), and PS (0.06 – 0.53 µg/L) nanoplastics. The presented analytical method offers an accurate means to identify, quantify, and monitor nanoplastics in complex environmental and potable water samples. It fills gaps in our understanding of nanoplastic pollution levels, providing a valuable methodology and crucial reference data for future studies. [Display omitted] • Presentation of a methodology for the quantification of nanoplastics in water. • Mass concentrations of nanoplastics across water samples were assessed by Pyr-GC/MS. • Eight nanoplastics (PMMA, Nylon 6, Nylon 66, PC, PS, PET, PP, PE) quantified. • PE, PET, PP and PS were the predominant nanoplastics. • Total nanoplastics concentrations of between 0.04 and 1.17 µg/L in water samples. [ABSTRACT FROM AUTHOR]

Abstract Fish ingestion of microplastic has been widely documented throughout freshwater, marine, and estuarine species. While numerous studies have quantified and characterized microplastic particles, analytical methods for polymer identification are limited. This study investigated the applicability of pyr-GC/MS for polymer identification of microplastics extracted from the stomach content of marine fish from the Texas Gulf Coast. A total of 43 microplastic particles were analyzed, inclusive of 30 fibers, 3 fragments, and 10 spheres. Polyvinyl chloride (PVC) and polyethylene terephthalate (PET) were the most commonly identified polymers (44.1%), followed by nylon (9.3%), silicone (2.3%), and epoxy resin (2.3%). Approximately 42% of samples could not be classified into a specific polymer class, due to a limited formation of pyrolytic products, low product abundance, or a lack of comparative standards. Diethyl phthalate, a known plasticizer, was found in 16.3% of the total sample, including PVC (14.3%), silicone (14.3%), nylon (14.3%), and sample unknowns (57.2%). Highlights • Pyr-GC/MS is an applicable tool for polymer identification of microplastic ingested by fish. • PVC and PET were the most commonly identified polymers. • Ingested microplastic may reflect local sources of pollution (e.g. petroleum waste). [ABSTRACT FROM AUTHOR]

This study aims to evaluate the chemical composition of wood and extractives ofPinus taedaandSchizolobium parahyba(guapuruvu) as potential feedstock for new applications in the biorefinery industry. For this purpose, their content ofα-cellulose, hemicellulose, insoluble lignin, hot water solubility, NaOH1%solubility, inorganic materials (ash), and monomeric sugars by high-performance liquid chromatography was quantified. Attenuated total reflectance infrared spectroscopy and thermogravimetric analysis were also used to complete the physicochemical characterization of the studied woods. The extractives were obtained by soxhlet extraction with ethanol:toluene and dichloromethane and identified with pyrolysis-gas chromatography/mass spectroscopy technique. The results showed that guapuruvu wood has the higher amount of hemicellulose (16%) when compared to pine wood (10%), which resulted in higher solubility in alkali solution. Furthermore, in relation to other biomasses, the two woods presented more percentage of lignin and minor content of hemicelluloses. TheP. taedawood presented the highest percentage of extractives mainly composed of fatty acids and aromatic hydrocarbons, while guapuruvu wood had a higher percentage of phenolic compounds and also fatty acids. Both the materials have low content of extractives with dichloromethane and were mainly composed of lipophilic compounds. [ABSTRACT FROM PUBLISHER]

This study aimed to characterize by analytical techniques Sideroxylon obtusifolium herbal medicine raw material derived from the leaves in different particle sizes, using scanning electron microscopy (SEM), thermoanalytical techniques [thermogravimetry (TG) and analysis differential thermal (DTA)] and pyrolysis coupled to gas chromatography/mass spectrometry (PYR-GC/MS). The different particle surface area among the samples was differentiated by the techniques. SEM distinguished the particles by its volumetric size, DTA and TG by the thermal and kinetic parameters and the PYR-GC/MS by degradation products chromatographic identification through the pyrograms. [ABSTRACT FROM AUTHOR]

Bioplastics are materials that are biobased and/or biodegradable, but not necessarily both. Concerns about environmental plastic pollution are constantly growing with increasing demand for substituting fossil-based plastics with those made using renewable resource feedstocks. For many conventional bioplastics to completely decompose/degrade, they require specific environmental conditions that are rarely met in natural ecosystems, leading to rapid formation of micro-bioplastics. As global bioplastic production and consumption/use continue to increase, there is growing concern regarding the potential for environmental pollution from micro-bioplastics. However, the actual extent of their environmental occurrence and potential impacts remains unclear, and there is insufficient mass concentration-based quantitative data due to the lack of quantitative analytical methods. This study developed and validated an analytical method coupling pressurized liquid extraction and pyrolysis-gas chromatography-mass spectrometry combined with thermochemolysis to simultaneously identify and quantify five targeted micro-bioplastics (i.e., polylactic acid (PLA), polyhydroxyalkanoate, polybutylene succinate, polycaprolactone, and polybutylene adipate terephthalate (PBAT)) in environmental samples on a polymer-specific mass-based concentration. The recovery of spiked micro-bioplastics in environmental samples (biosolids) ranged from 74 to 116%. The limits of quantification for the target micro-bioplastics were between 0.02 and 0.05 mg/g. PLA and PBAT were commonly detected in wastewater, biosolids, and sediment samples at concentrations between 0.07 and 0.18 mg/g. The presented analytical method enables the accurate identification, quantification, and monitoring of micro-bioplastics in environmental samples. This study quantified five micro-bioplastic types in complex environmental samples for the first time, filling in gaps in our knowledge about bioplastic pollution and providing a useful methodology and important reference data for future research.

Analytical techniques have been used to characterize compounds from herbal medicine, its products and extracts. The objective of this study was to characterize a variety of particle sizes of Erythrina velutina Willd powder. The samples used in the study were named MUF01 (710 μm), MUF03 (180 μm) and MUF05 (75 μm). The techniques employed were scanning electron microscopy (SEM), thermal analysis such as thermogravimetry (TG) and differential thermal analysis (DTA) together with pyrolysis coupled to gas chromatography/mass spectrometry (Pyr-GC/MS). SEM enabled us to detect the existence of divergences from the expected results from the granulometry process. Thermal analytical techniques (TG and DTA) showed the thermal decomposition profile, corresponding to physical and chemical phenomena. The chromatographic data relative to the peak area of the compounds analyzed evidenced quantitative differences in the chemical compositions of the samples MUF01, MUF03, and MUF05 at 300, 450 and 600 °C. Neophytadiene 2,6,10-trimethyl, 14 and 3-eicosyne were identified by Pyr-GC/MS at 300, 450 and 600 °C, and it classified the samples according the peak area values, which were MUF05 > MUF03 > MUF01. SEM, DTA and TG confirmed this through particle size uniformity, heat flow, and mass loss, respectively. [ABSTRACT FROM AUTHOR]

Microplastics (1 - 5000 µm) are pervasive in every compartment of our environment. However, little is understood regarding the concentration and size distribution of microplastics in road dust, and how they change in relation to human activity. Within road dust, microplastics move through the environment via atmospheric transportation and stormwater run-off into waterways. Human exposure pathways to road dust include dermal contact, inhalation and ingestion. In this study, road dust along an urban to rural transect within South-East Queensland, Australia was analysed using Accelerated Solvent Extraction followed by pyrolysis Gas Chromatography-Mass Spectrometry (Pyr-GC/MS). Polypropylene, polystyrene, polyethylene terephthalate, polyvinyl chloride, poly (methyl methacrylate) and polyethylene were quantified. Microplastic concentrations ranged from ~0.5 mg/g (rural site) to 6 mg/g (Brisbane city), consisting primarily of polyvinyl chloride (29%) and polyethylene terephthalate (29%). Size fractionation (< 250 µm, 250–500 µm, 500–1000 µm, 1000–2000 µm and 2000–5000 µm) established that the < 250 µm size fraction contained the majority of microplastics by mass (mg/g). Microplastic concentrations in road dust demonstrated a significant relationship with the volume of vehicles (r2 = 0.63), suggesting traffic, as a proxy for human movement, is associated with increased microplastic concentrations in the built environment. [Display omitted] • Street dust from Queensland, Australia was sampled in a city to rural transect. • Microplastics of PP, PS, PET, PVC, PMMA and PE were quantified using (pyr-GC/MS). • Concentrations ranged from ~0.5 mg/g (Rural) to 6 mg/g (City location). • Polyvinyl chloride (29%) and polyethylene terephthalate (29%) were the most abundant of all quantified microplastic. • Concentrations correlated with traffic volumes. (r2 = 0.63). [ABSTRACT FROM AUTHOR]

• Archived biosolids from australia and UK from 1950 to 2016 analyzed for 7 plastics. • Increasing concentrations over time of PP, PS, PET, PMMA, PVC and PE. • Prior to the 1990s, leakage of plastics into biosolids was limited except for PS. • Leakage from 1990s driven by increased production and consumption of PE, PET, PVC. • Concentrations of plastics closely correlate with production and consumption. Plastics are ubiquitous contaminants that leak into the environment from multiple pathways including the use of treated sewage sludge (biosolids). Seven common plastics (polymers) were quantified in the solid fraction of archived biosolids samples from Australia and the United Kingdom from between 1950 and 2016. Six plastics were detected, with increasing concentrations observed over time for each plastic. Biosolids plastic concentrations correlated with plastic production estimates, implying a potential link between plastics production, consumption and leakage into the environment. Prior to the 1990s, the leakage of plastics into biosolids was limited except for polystyrene. Increased leakage was observed from the 1990s onwards; potentially driven by increased consumption of polyethylene, polyethylene terephthalate and polyvinyl chloride. We show that looking back in time along specific plastic pollution pathways may help unravel the potential sources of plastics leakage into the environment and provide quantitative evidence to support the development of source control interventions or regulations. [Display omitted] [ABSTRACT FROM AUTHOR]

Microplastics (MPs) quantification in benthic marine sediments is typically performed by time-consuming and moderately accurate mechanical separation and microscopy detection. In this paper, we describe the results of our innovative Polymer Identification and Specific Analysis (PISA) of microplastic total mass, previously tested on either less complex sandy beach sediment or less demanding (because of the high MPs content) wastewater treatment plant sludges, applied to the analysis of benthic sediments from a sublittoral area north-west of Leghorn (Tuscany, Italy). Samples were collected from two shallow sites characterized by coarse debris in a mixed seabed of Posidonia oceanica, and by a very fine silty-organogenic sediment, respectively. After sieving at <2 mm the sediment was sequentially extracted with selective organic solvents and the two polymer classes polystyrene (PS) and polyolefins (PE and PP) were quantified by pyrolysis-gas chromatography-mass spectrometry (Pyr-GC/MS). A contamination in the 8–65 ppm range by PS could be accurately detected. Acid hydrolysis on the extracted residue to achieve total depolymerization of all natural and synthetic polyamides, tagging of all aminated species in the hydrolysate with a fluorophore, and reversed-phase high performance liquid chromatography (HPLC) (RP-HPLC) analysis, allowed the quantification within the 137–1523 ppm range of the individual mass of contaminating nylon 6 and nylon 6,6, based on the detected amounts of the respective monomeric amines 6-aminohexanoic acid (AHA) and hexamethylenediamine (HMDA). Finally, alkaline hydrolysis of the residue from acid hydrolysis followed by RP-HPLC analysis of the purified hydrolysate showed contamination by polyethylene terephthalate (PET) in the 12.1–2.7 ppm range, based on the content of its comonomer, terephthalic acid. [ABSTRACT FROM AUTHOR]

An emission source of microplastics into the environment is laundering synthetic textiles and clothing. Mechanical drying as a pathway for emitting microplastics, however, is poorly understood. In this study, emissions of microplastic fibres were sampled from a domestic vented dryer to assess whether mechanical drying of synthetic textiles releases microplastic fibres into the surrounding air or are captured by the inbuilt filtration system. A blue polyester fleece blanket was repeatedly washed and dried using the 'Normal Dry' program of a common domestic dryer operated at temperatures between 56 and 59 °C for 20 min. Microfibres in the ambient air and during operation of the dryer were sampled and analysed using microscopy for particle quantification and characterisation followed by Fourier-Transform Infrared Spectroscopy (FTIR) and Pyrolysis Gas Chromatography-Mass Spectrometry (Pyr-GC/MS) for chemical characterisation. Blue fibres averaged 6.4 ± 9.2 fibres in the room blank (0.17 ± 0.27 fibres/m3), 8.8 ± 8.5 fibres (0.05 ± 0.05 fibres/m3) in the procedural blank and 58 ± 60 (1.6 ± 1.8 fibres/m3) in the sample. This is the first study to measure airborne emissions of microplastic fibres from mechanical drying, confirming that it is an emission source of microplastic fibres into air – particularly indoor air. Unlabelled Image • Emissions of microplastic fibres from residential dryers into air investigated. • Mechanical drying of polyester emits microplastic fibres into the surrounding air. • Over 20 mins operation, MP emissions for a 660 g blanket were ~ 1.6–1.8 fibres/m3. • Lint of 77 ± 22.4 mg ≈ 1.1 × 106 ± 3.2 × 105 fibres captured by inbuilt filtration. • Lint emissions were approximately 0.012% of the blanket mass/wash. [ABSTRACT FROM AUTHOR]