Evidence shows that the majority of aquatic field microplastics (MPs) could be microfibers (MFs) which can be originated directly from massive sources such as textile production and shedding from garments, agricultural textiles and clothes washing. In addition, wear and tear of tyres (TRWPs) emerges as a stealthy major source of micro and nanoplastics, commonly under-sampled/detected in the field. In order to compile the current knowledge in regards to these two major MPs sources, concentrations of concern in aquatic environments, their distribution, bulk emission rates and water mitigation strategies were systematically reviewed. Most of the aquatic field studies presented MFs values above 50%. MPs concentrations varied from 0.3 to 8925 particles m⁻³ in lakes, from 0.69 to 8.7 × 10⁶ particles m⁻³ in streams and rivers, from 0.16 to 192000 particles m⁻³ estuaries, and from 0 to 4600 particles m⁻³ in the ocean. Textiles at every stage of production, use and disposal are the major source of synthetic MFs to water. Laundry estimates showed an averaged release up to 279972 tons year⁻¹ (high washing frequency) from which 123000 tons would annually flow through untreated effluents to rivers, streams, lakes or directly to the ocean. TRWPs in the aquatic environments showed concentrations up to 179 mg L⁻¹ (SPM) in runoff river sediments and up to 480 mg g⁻¹ in highway runoff sediments. Even though average TRWR emission is of 0.95 kg year⁻¹ per capita (10 nm- 500 μm) there is a general scarcity of information about their aquatic environmental levels probably due to no-availability or inadequate methods of detection. The revision of strategies to mitigate the delivering of MFs and TRWP into water streams illustrated the importance of domestic laundry retention devices, Waste Water Treatment Plants (WWTP) with at least a secondary treatment and stormwater and road-runoff collectors quality improvement devices.

Clothes may contain a large range of chemical additives and other toxic substances, which may eventually pose a significant risk to human health. Since they are associated with pigments, polychlorinated biphenyls (PCBs) may be especially relevant. On the other hand, infants are very sensitive to chemical exposure and they may wear some contact and colored textiles for a prolonged time. Consequently, a specific human health risk assessment is required. This preliminary study was aimed at analyzing the concentrations of PCBs in ten bodysuits purchased in on-line stores and local retailers. The concentrations of 12 dioxin-like and 8 non-dioxin-like PCB congeners were determined by gas chromatography coupled to high resolution mass spectrometry, with detection limits ranging between 0.01 and 0.13 pg/g. The dermal absorption to PCBs of children at different ages (6 months, 1 year and 3 years old) was estimated, and the non-cancer and cancer risks were evaluated. Total levels of PCBs ranged from 74.2 to 412 pg/g, with a mean TEQ concentration of 13.4 pg WHO-TEQ/kg. Bodysuits made of organic cotton presented a total mean PCB concentration substantially lower than clothes made of regular cotton (11.0 vs. 15.8 pg WHO-TEQ/kg). The dermal absorption to PCBs for infants was calculated in around 3·10⁻⁵ pg WHO-TEQ/kg·day, regardless the age. This value is > 10,000-fold lower than the dietary intake of PCBs, either through breastfeeding or food consumption. Furthermore, this exposure value would not pose any health risks for the infants wearing those bodysuits. Anyhow, as it is a very preliminary study, this should be confirmed by analyzing larger sets of textile samples. Further investigations should be also focused on the co-occurrence of PCBs and other toxic chemicals (i.e., formaldehyde, bisphenols and aromatic amines) in infant clothes.

Microplastic fibers (MP) from textile weathering and washing are increasingly being recognized as environmental pollutants. The majority of studies on the bioavailability and effects of microplastic focused on small polystyrene spherical plastic particles, while less data are available for fibers and for other materials besides polystyrene. We investigated the ingestion and effects of ground polyethylene terephthalate (PET) textile microfibers (length range: 62–1400 μm, width 31–528 μm, thickness 1–21.5 μm) on the freshwater zooplankton crustacean Daphnia magna after a 48 h exposure and subsequent 24 h of recovery in MP free medium and algae. The majority of ingested fibers by D. magna were around 300 μm, but also some very large twisted MP fibers around 1400 μm were found inside the gut. Exposure to these fibers results in increased mortality of daphnids after 48 h only in the case where daphnids were not pre-fed with algae prior to experiment, but no effect was found when daphnids were fed before the experiments. Regardless of the feeding regime, daphnids were not able to recover from MP exposure after additional 24 h incubation period in a MP free medium with algae. The uptake and effects of PET textile MP on D. magna are presented here for the first time.

Microplastics (synthetic polymers <5 mm) have been recently recognized as a big environmental concern, as their ubiquity is an undeniable fact. Their wide variety regarding shapes, sizes, and materials turn them into an intrinsically risky pollutant capable of causing several environmental impacts. Textile microfibers (MF) are a microplastic sub-group. These are mostly shed when a normal laundry of any garment takes place. Special attention has been put onto them, as high concentrations have been found in products for human consumption as shellfish and tap water. However, as there is no consensus on the methodologies to quantify and report the results of MFs detached from textile garments, the degree of similarity between published studies is very low. Hence, the aim of this research was to evaluate the microfibers’ detachment rates of finished garments and to provide a set of comparable units to report the results. These were found to range between 175 and 560 MF/g or 30000–465000 MF/m² of garment. In addition, there was a high correlation between the MF detachment and the textile article superficial density. Finally, our results were compared with a recent paper that estimated the annual mass flow of MFs to the oceans. This previous publication is 30 times higher when related to the mass but 40 times lower if related to the number of MFs.

This is a study of the sources of alkylphenol and alkylphenol ethoxylates in wastewater, including the new observation that the main contribution is from textiles. Alkylphenols and alkylphenol ethoxylates are widely used chemicals in various applications that are partly under environmental restrictions within Europe. The study sets out to analyze the most important sources of this large group of organic compounds in an urban wastewater system. A substance flow analysis (SFA) of the technosphere in Stockholm, Sweden in 2004 was conducted, allowing a comparison of 13 groups of goods' emissions to wastewater. It was found that the groups of textiles and cleaning agents were the major sources to wastewater, while the group's personal care products and paint and lacquers give smaller contributions. The content of alkylphenol ethoxylates in goods, especially in textiles, is a most significant source and is probably valid for other urban areas as well.

This study investigates the effect of low molecular weight carboxylic acid on degradation of textile dye C.I. Reactive Orange 16 (RO16), in function of initial pH, using Ultra Violet light and H2O2. Experiments were performed in photoreactor with UVC lamps in stationary conditions. Results shows that carboxylic acids have inhibitory effect on degradation process of dye. With increasing concentration of dye inhibitory effect grows. Inhibitory effect of acid are higher on pH values of solution higher than pKa acids, because than in solution acids appear almost entirely in the form of anion. The highest inhibitory effect shows formates, smaller propanoates, and the smallest acetates. UV/H2O2 process is very effective for removal of organic pollutants, but the efficiency of this process was significantly lower in the presence of lower carboxylic acids.