{"id":37174,"date":"2025-12-10T18:21:31","date_gmt":"2025-12-10T17:21:31","guid":{"rendered":"https:\/\/www.vtei.cz\/?p=37174"},"modified":"2026-02-12T13:00:36","modified_gmt":"2026-02-12T12:00:36","slug":"pfas-in-surface-waters-in-the-czech-republic","status":"publish","type":"post","link":"https:\/\/www.vtei.cz\/en\/2025\/12\/pfas-in-surface-waters-in-the-czech-republic\/","title":{"rendered":"Current status of monitoring selected PFAS in surface waters in the Czech Republic"},"content":{"rendered":"<h2>ABSTRACT<\/h2>\n<p>Per- and polyfluorinated compounds (PFAS), a group of fluorinated compounds of anthropogenic origin, have been classified as a persistent organic substances of significant concern due to their chemical properties, widespread use in a number of industrial sectors, environmental spread, long term bioaccumulation potential, and resulting risk to human health. This article brings an overview of current knowledge about the occurrence of PFAS in the environment, mainly in surface, ground, and drinking water and about the methods of their removal from contaminated water. Furthermore, the legislative requirements regarding PFAS at the level of the EU and Czech Republic are summarised here, including the list of compounds according to the Directive of the European Parliament and the Council 2020\/2184 and the Proposal for a Directive of the European Parliament and the Council 2008\/105\/EC.<br \/>\nThe article also includes an overview of analytical methods for determination of PFAS, including trifluoroacetic acid (TFA), and the determination of total organic fluorine. The methods are generally based on liquid chromatography coupled with mass detection. Differences are primarily in sample pre-treatment. The main attention is focused on a summary of relevant data PFAS monitoring in surface water from all Czech Republic territory. Until 2022, only perfluorooctane sulfonic acid (PFOS) and (except for the Odra and Oh\u0159e basins) perfluorooctanoic acid (PFOA) were consistently monitored in surface waters in the Czech Republic. Detection limits of methods used in individual basins were different; therefore, an objective summary of relevant data about PFAS monitoring in the Czech Republic is impossible. Methodologies enabling determination with higher sensitivity and, in particular, a wider range of monitored substances are gradually being introduced with the expansion of analytical possibilities. From 2023, monitoring of substances from PFAS group compounds was introduced in individual basins on a wider scale, including pilot monitoring, which is presented in this article.<\/p>\n<h2>INTRODUCTION<\/h2>\n<p>The\u00a0history of\u00a0per- and polyfluorinated substances (PFAS), the\u00a0so-called \u201cforever\u201d chemicals, began\u00a0in\u00a01938, when the\u00a0chemist Roy J. Plunkett, an\u00a0employee of\u00a0DuPont, accidentally discovered polytetrafluoroethylene (PTFE) during the\u00a0manufacture of\u00a0Freon. This new fluorinated plastic was patented by Kinetic Chemicals in\u00a01941 (U.S. Patent 2,230,654) [1], and in\u00a01945 the\u00a0trademark Teflon was registered [2]. More than\u00a07,000,000 compounds fall within\u00a0the\u00a0PFAS group. In\u00a0order to unify and harmonise communication on PFAS among scientific, regulatory and industrial communities, recommended names, acronyms, structural formulae and CAS Registry Numbers have been proposed [3]. The\u00a0OECD has identified more than\u00a04,700 compounds on the\u00a0basis of\u00a0their CAS numbers [4]. PTFE, however, is not a\u00a0fully typical compound. PFAS include PFOS (perfluorooctane sulfonic acid) and PFOA (perfluorooctanoic acid), which were first detected in\u00a0the\u00a01950s during the\u00a0production of\u00a0Teflon.<\/p>\n<h3>Current state of\u00a0knowledge<\/h3>\n<p>PFAS have attracted considerable attention over the\u00a0past 10 to 15 years. Thanks to their lyophobic and hydrophobic nature, they have found wide use in\u00a0a\u00a0range of\u00a0sectors, for example in\u00a0the\u00a0textile and leather industries, in\u00a0fire-fighting foams, surface protection agents, household products, food-contact packaging, the\u00a0photographic industry, aviation hydraulic fluids, electroplating, and as surfactants in\u00a0pesticides and other agricultural chemicals [5]. In\u00a0the\u00a01990s, these substances were identified at low concentrations in\u00a0all parts of\u00a0the\u00a0environmental (water, soil, air, plants, living organisms) thanks to the\u00a0development of\u00a0analytical methods for their determination and advances in\u00a0instrumentation, particularly the\u00a0emergence of\u00a0liquid chromatography coupled with mass spectrometry [3, 6].<\/p>\n<p>Due to the\u00a0significant expansion of\u00a0PFAS production, there has also been an\u00a0increase since 2000 in\u00a0publications addressing this group of\u00a0substances, their sources and fate in\u00a0the\u00a0environment, and their harmful effects. In\u00a02020, nearly 1,000\u00a0publications dealing with this issue were published [6].<\/p>\n<p>The\u00a0toxicity of\u00a0PFAS to humans and their impact on ecosystems currently receive extraordinary attention. An\u00a0increasing number of\u00a0substances from this group are being monitored regularly, and concentrations considered safe are decreasing. There is a\u00a0need to gain\u00a0a\u00a0better understanding of\u00a0the\u00a0fate and impacts of\u00a0these persistent chemicals on the\u00a0environment, as it can\u00a0be assumed that the\u00a0burden on surface and groundwater by these substances is underestimated [7]. A\u00a0publication by the\u00a0authors of\u00a0the\u00a0current article [8] addresses a\u00a0range of\u00a0existing information on the\u00a0applications, environmental release, and remediation technologies of\u00a0per- and polyfluoroalkyl substances.<\/p>\n<p>In\u00a0connection with the\u00a0regulation and restriction of\u00a0PFAS use, attention should also be paid to alternative substances, the\u00a0monohydrogen-substituted perfluoroalkyl carboxylic acids (H-PFAS), which are also found in\u00a0surface waters. In\u00a0the\u00a0Netherlands, a\u00a0UHPLC-MS\/MS method was developed, validated, and applied for the\u00a0determination of\u00a0these contaminants in\u00a0surface water samples [9].<\/p>\n<p>Very little information is currently available on the\u00a0PFOA substitute known as GenX. Despite its lower bioaccumulative potential, this alternative substance may still pose a\u00a0risk to both the\u00a0environment and human\u00a0health [10].<\/p>\n<p>Given the\u00a0global distribution of\u00a0these chemicals, studies have been conducted to monitor their presence in\u00a0developing countries in\u00a0water samples and other samples from the\u00a0abiotic environment and biota. PFAS were identified in\u00a072 % of\u00a0the\u00a0samples [11, 12].<\/p>\n<p>PFAS clearly represent a\u00a0global problem. Levels of\u00a0four selected perfluoroalkyl acids (PFAA) \u2013 perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA), perfluorohexane sulfonic acid (PFHxS), and perfluorononanoic acid (PFNA) \u2013 have been tested in\u00a0various global environmental media, namely rainwater, soils, and surface waters. Among other findings, it has been shown that PFOS levels in\u00a0rainwater in\u00a0some inland areas of\u00a0the\u00a0European\u00a0Union often exceed the\u00a0environmental quality standard for surface waters. It is therefore crucial that the\u00a0use of\u00a0these substances is restricted as rapidly as possible [13, 14].<\/p>\n<p>Current efforts by the\u00a0European\u00a0Commission to initiate discussions on the\u00a0largest proposal to restrict PFAS in\u00a0history reflect the\u00a0poor global situation regarding PFAS accumulation in\u00a0the\u00a0environment and their health impacts. However, a\u00a0comprehensive analysis is still lacking. Interest in\u00a0the\u00a0issue has been successfully raised, with the\u00a0focus of\u00a0research gradually shifting towards ecological questions. The\u00a0involvement of\u00a0developing countries, however, is limited, despite the\u00a0fact that PFAS exposure in\u00a0these regions is extremely high. It is therefore necessary to pursue globally interconnected and multidisciplinary approaches to address issues related to PFAS [15]. Other studies also provide a\u00a0critical review of\u00a0the\u00a0global occurrence and distribution of\u00a0these persistent chemicals in\u00a0waters, including wastewater [16, 17].<\/p>\n<p>In\u00a0Sweden, PFAS have been detected in\u00a0both raw and drinking water, as well as in\u00a0groundwater [18, 19].<\/p>\n<p>In\u00a0the\u00a0Czech Republic, PFAS were tested in\u00a0tap water. In\u00a0192 drinking water samples from across the\u00a0country, 28 PFAS were analysed using high-performance liquid chromatography coupled with tandem mass spectrometry following solid-phase extraction. It was found that the\u00a0occurrence of\u00a0PFAS in\u00a0drinking water in\u00a0the\u00a0Czech Republic is very low compared with other European\u00a0studies. Approximately 1 % of\u00a0the\u00a0analysed samples could present a\u00a0potential health risk [20, 21]. In\u00a0seven locations on the\u00a0Svitava and Svratka rivers in\u00a0the\u00a0Brno urban\u00a0development, the\u00a0occurrence of\u00a0perfluorinated substances in\u00a0water and fish blood plasma was monitored. Concentrations of\u00a0PFHxS, FHUEA, FOSA, and N-methyl FOSA were below the\u00a0detection limits. The\u00a0main\u00a0component in\u00a0fish blood was PFOS, followed by PFNA and PFOA. In\u00a0water, the\u00a0primary detected compound was PFOA, followed by PFOS and PFNA. A\u00a0significant correlation was observed between PFOA concentrations in\u00a0blood plasma and in\u00a0water (r\u202f=\u202f0.74) [22]. Arnika has also monitored the\u00a0occurrence of\u00a0PFAS together with brominated flame retardants in\u00a0Prague and its surroundings. High concentrations were measured in\u00a0the\u00a0Kopaninsk\u00fd stream. The\u00a0values were significantly higher than\u00a0those commonly found in\u00a0surface waters in\u00a0Europe. In\u00a0this case, the\u00a0source of\u00a0pollution may be V\u00e1clav Havel Airport [23].<\/p>\n<p>As early as 2010, contamination of\u00a0the\u00a0Rhine river was monitored. Seventy-five water samples were collected along the\u00a0entire course of\u00a0the\u00a0Rhine river, from Lake Constance to the\u00a0North Sea, including several major tributaries such as the\u00a0Neckar, Main, and Ruhr rivers, and waters from the\u00a0Rhine\u2013Meuse delta, specifically the\u00a0Meuse and Scheldt rivers. The\u00a0aim was to identify possible sources of\u00a0contamination [24].<\/p>\n<p>PFAS were also monitored in\u00a0the\u00a0Danube river basin. A\u00a0total of\u00a082 PFAS and 72 other suspected compounds were identified in\u00a095 samples. Many of\u00a0the\u00a0substances detected are not currently regulated [25].<\/p>\n<p>With the\u00a0increasing information on toxicity and population exposure, concerns arose regarding the\u00a0impact on human\u00a0health. Several studies have been conducted examining the\u00a0relationship between PFAS concentrations in\u00a0blood serum and in\u00a0drinking water [26, 27]. PFAS have also been detected in\u00a0breast milk and infant formula [28].<\/p>\n<p>Trifluoroacetic acid (TFA), which belongs to the ultrashort-chain subgroup of PFAAs, is included in the revised European Commission directives. It is a highly persistent compound, with concentrations in parts of the environment (soil, water, air, plants, plant-based foods, and human serum) increasing significantly. TFA is a transformation product of many PFAS and is also released into the environment from industrial TFA production. Studies on the occurrence of TFA in the environment, including surface waters, show that over the past 20 years its concentrations in all parts of the environment have increased severalfold and are currently many times higher than those of other per- and polyfluoroalkyl substances. Data on the toxicity and ecotoxicity of TFA are limited, but it is nevertheless clear that there is a potential global risk of its irreversible accumulation [29, 30].<\/p>\n<h3>Removal of PFAS from wastewater<\/h3>\n<p>One of the key tasks is to identify a suitable sorbent for removing PFAS from contaminated water. Biochar appears to be a cost-effective and environmentally friendly adsorbent for the elimination of PFAS [31]. Other potential methods for removing not only perfluorinated substances include ozonation, granular activated carbon, and membrane processes using reverse osmosis. However, PFAS were not removed by ozonization; these chemicals were effectively eliminated using physical methods, such as adsorption on activated carbon and processes based on reverse osmosis membranes [32]. Several magnetic materials, including iron oxides, ferrites, and magnetic carbon composites, also appear to be effective adsorbents for the removal of PFAS from water. These substances have demonstrated considerable potential for use in various environmental remediation applications, as well as in the treatment of PFAS-contaminated water [33]. Mixed-matrix membrane technology removes more than 99 % of PFAS from wastewater [34]. A concise summary of the occurrence, transformation, and removal of poly- and perfluoroalkyl substances in wastewater treatment plants (WWTPs) was prepared by Lenka et\u202fal. [35]. They also highlight that information on PFAS is particularly scarce for developing countries. Another study provides a comprehensive review of PFAS sources and their remediation [36].<\/p>\n<p>Another study focused on the\u00a0fate and transport of\u00a0PFAS and inorganic fluoride in\u00a0a\u00a0municipal WWTP operating a\u00a0sewage sludge incinerator (SSI). A\u00a0robust statistical analysis characterised concentrations and mass flows across all primary influents and effluents of\u00a0the\u00a0WWTP and SSI, including emissions from thermal treatment into the\u00a0air. A\u00a0PFAS removal efficiency of\u00a051 % indicates that the\u00a0SSI can\u00a0only partially eliminate PFAS [37]. An\u00a0overview of\u00a0the\u00a0current state of\u00a0research on treatment technologies suitable for the\u00a0removal of\u00a0PFAS from the\u00a0environment, particularly from water, is provided in\u00a0the\u00a0publication Per- and Polyfluoroalkyl Substances Treatment Technologies [38].<\/p>\n<h3>PFAS Legislation at the EU and Czech Republic levels<\/h3>\n<p>Legislative instruments are the primary means of limiting perfluorinated organic compounds in the environment. One of the first measures was the inclusion of selected perfluorinated organic compounds on the list of persistent organic pollutants (POPs) under the Stockholm Convention [39]. Under Article\u202f3 of the Convention, parties and organisations (signatories) are required to prohibit and\/or adopt the legal and administrative measures necessary to eliminate: the production and use of the chemicals listed in Annex\u202fA; the import and export of the chemicals listed in Annex\u202fA; and to restrict the production and use of the chemicals listed in Annex\u202fB of the Convention. The Annex\u202fA list (Elimination) of the Stockholm Convention includes perfluorohexane sulfonic acid (PFHxS), its salts, and related compounds that may potentially degrade to PFHxS, as well as perfluorooctanoic acid (PFOA), its salts, and related compounds that may potentially degrade to PFOA. In the case of PFOA, certain uses or products are subject to specific exemptions, including applications in the photographic industry, some medical uses, the textile industry (production of protective clothing for environments where there is a risk of adverse effects on human health), and in fire-fighting foams for the suppression of flammable liquid vapours and the extinguishing of flammable liquid fires (Class\u202fB fires). However, by 2025 at the latest, the use of fire-fighting foams containing or potentially containing PFOA, its salts, and PFOA-related compounds must be restricted to locations where all releases can be fully captured. The Annex\u202fB list (Restriction) of the Stockholm Convention includes\u00a0perfluorooctane sulfonic acid (PFOS), its salts, and perfluorooctane sulfonyl fluoride. Use is permitted in\u00a0electroplating processes within\u00a0closed systems, in\u00a0fire-fighting foams for the\u00a0suppression of\u00a0flammable liquid vapours and the\u00a0extinguishing of\u00a0flammable liquid fires (Class\u202fB fires), and in\u00a0insect baits containing the\u00a0active substance sulfluramid (CAS\u202fno.\u202f4151\u201150\u20112) for the\u00a0control of\u00a0ants of\u00a0the\u00a0genera Atta spp. and Acromyrmex spp., strictly for agricultural purposes.<\/p>\n<p>Another measure is Regulation (EU) 2019\/1021\u00a0 of the European Parliament and of the Council [40], which sets restrictive conditions for the use or placing on the market of products containing perfluorinated substances within the European Union. According to Article\u202f3 of this Regulation, the manufacture, placing on the market, and use of the substances listed in Annex\u202fI \u2013 whether as such, in mixtures, or in articles \u2013 are prohibited. In the case of PFOS, its salts, and related substances that degrade to PFAS, these substances may be present in mixtures or articles only as unintentional trace contaminants (Article\u202f4, paragraph\u202f1(b)), in quantities specified in Annex\u202fI to the Regulation. This annex has been amended several times for PFOS to tighten the limits on unintentional contamination. The use of PFOS in hexavalent chromium (Cr<sup>6+<\/sup>) electroplating processes in\u00a0closed systems was permitted until 7\u00a0September\u202f2025. A\u00a0Member State could apply for an\u00a0exemption for the\u00a0above purpose by 7\u00a0September\u202f2024, which could be granted for a\u00a0maximum period of\u00a0five years. Under an\u00a0exemption pursuant to Regulation 2019\/1021, the\u00a0manufacture, placing on the\u00a0market, and use of\u00a0PFOA, its salts, and PFOA-related compounds could be authorised for the\u00a0following purposes:<\/p>\n<hr \/>\n<ol style=\"list-style-type: upper-alpha;\">\n<li>photolithographic production and etching processes in\u00a0semiconductor manufacturing, until 4\u00a0July\u202f2025;<br \/>\n<hr \/>\n<\/li>\n<li>photographic coatings applied to films, until 4\u00a0July\u202f2025;<br \/>\n<hr \/>\n<\/li>\n<li>oil- and water-resistant textiles for the\u00a0protection of\u00a0workers against hazardous liquids posing a\u00a0risk to their health and safety, until 4\u00a0July\u202f2023;<br \/>\n<hr \/>\n<\/li>\n<li>invasive and implantable medical devices, until 4 July\u202f2025<br \/>\n<hr \/>\n<\/li>\n<li>the\u00a0manufacture of\u00a0polytetrafluoroethylene (PTFE) and polyvinylidene fluoride (PVDF) for the\u00a0production of:\n<ul>\n<li>high-performance, corrosion-resistant membranes for gas filtration, water filtration, and medical textile applications,<\/li>\n<li>equipment for heat exchangers to recover heat from industrial waste,<\/li>\n<li>industrial sealing materials capable of\u00a0preventing the\u00a0release of\u00a0volatile organic compounds and PM2.5 (particulate matter 2.5) into the\u00a0environment, until 4\u00a0July\u202f2023;<br \/>\n<hr \/>\n<\/li>\n<\/ul>\n<\/li>\n<li>In\u00a0fire-fighting foam for the\u00a0suppression of\u00a0vapours released from flammable liquids and for extinguishing flammable liquid fires (Class\u202fB fires), until 3\u00a0December\u202f2025.<\/li>\n<\/ol>\n<p>However, a\u00a0number of\u00a0products containing PFAS that were placed on the\u00a0market prior to the\u00a0entry into force of\u00a0the\u00a0above Regulation are still in\u00a0circulation (in\u00a0use).<\/p>\n<p>Derivatives of the above-mentioned substances are also subject to restrictions under REACH [41]. These include, for example, ammonium perfluorohexane sulfonate or tridecafluorohexane sulfonic acid in a 1:1 mixture with 2,2\u2019-iminodiethanol. Perfluorobutanesulfonic acid (PFBS) is classified as a substance of very high concern [42]. In 2024, Commission Regulation (EU) 2024\/2462 [43] established new restrictive conditions concerning perfluorohexanoic acid (PFHxA), its salts, and related substances that may degrade to PFHxA. From 10 April\u202f2026, the placing on the market or use of fire-fighting foams and foam concentrates for public fire brigades containing PFHxA and its salts at concentrations equal to or greater than 25\u202fppb, or PFHxA-related substances at concentrations equal to or greater than 1,000\u202fppb, will be prohibited \u2013 except where these brigades respond to industrial fires at facilities covered by European Parliament and Council Directive 2012\/18\/EU [44]. From 10 October\u202f2029, the same restrictions will apply to fire-fighting foams and foam concentrates used in civil aviation. From 10 October\u202f2026, PFHxA may no longer be placed on the market or used at the above concentrations in textiles, leather, furs, and hides, in clothing and related accessories for the general public, in footwear for the general public, in paper and cardboard materials intended to come into contact with food under the scope of Regulation (EC)\u202fNo\u202f1935\/2004 [45], in mixtures for the general public, and in cosmetic products as defined in Article\u202f2(1)(a) of\u00a0Regulation (EC)\u202fNo\u202f1223\/2009 [46].<\/p>\n<p>In\u00a0the\u00a0area of\u00a0human\u00a0health protection, European\u00a0Parliament and Council Directive 2020\/2184 [47] was adopted at the\u00a0EU level, which in\u00a0Annex\u202fI, Part\u202fB, sets limit values for perfluorinated substances in\u00a0water intended for human\u00a0consumption. The\u00a0limit values are established for the\u00a0sum of\u00a020 selected perfluorinated substances (0.1\u202f\u00b5g\/l) or for total PFAS, including the\u00a0sum of\u00a0all per- and polyfluoroalkyl substances (0.5\u202f\u00b5g\/l). Member States are required to take the\u00a0necessary measures to comply with the\u00a0above limits by 12\u00a0January\u202f2026. These substances are monitored when, following a\u00a0risk assessment and management of\u00a0catchment areas related to abstraction points carried out in\u00a0accordance with Article\u202f8 of\u00a0the\u00a0Directive, it is concluded that the\u00a0presence of\u00a0these substances in\u00a0the\u00a0water source is probable.<\/p>\n<p>As of\u00a0June\u202f2024, the\u00a0European\u00a0Commission prepared an\u00a0amendment to several EU water policy directives [48]. The\u00a0amendment to European\u00a0Parliament and Council Directive 2008\/105\/EC proposes a\u00a0new list of\u00a0priority substances for the\u00a0aquatic environment, along with the\u00a0corresponding environmental quality standards (EQS). Under number 65, a\u00a0group of\u00a0per- and polyfluoroalkyl substances (PFAS) was listed, comprising 24 chemical perfluorinated compounds. For this sum of\u00a0PFAS, an\u00a0EQS has been set \u2013 annual average (EQS\u2011AA) of\u00a00.0044\u202f\u00b5g\/l (4.4\u202fng\/l) for the\u00a0surface water matrix and 0.077\u202f\u00b5g\/kg wet weight for biota. In\u00a0contrast to Directive 2020\/2184, the\u00a0amendment to Directive 2008\/105\/EC assigns a\u00a0conversion factor for each PFAS relative to perfluorooctane sulfonic acid (PFOS\u202f=\u202f1), against which the\u00a0toxic risk of\u00a0each additional PFAS is assessed. The\u00a0analytically determined concentration of\u00a0each PFAS is then multiplied by its respective factor, and the\u00a0resulting sum is compared with the\u00a0EQS. It should be noted that the\u00a0PFAS lists in\u00a0Directives 2020\/2184 and 2008\/105\/EC do not fully overlap; 16 PFAS are common to both lists (<em>Tab.\u202f1<\/em>).<\/p>\n<h5>Tab. 1. Comparison of lists of PFAS substances according to Directive 2020\/2184 of the European Parliament and of the Council and the draft amendment of Directive 2008\/105\/EC of\u00a0the\u00a0European\u00a0Parliament and of\u00a0the\u00a0Council<\/h5>\n<a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-1-1.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-37143 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-1-1.jpg\" alt=\"\" width=\"800\" height=\"758\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-1-1.jpg 800w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-1-1-300x284.jpg 300w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-1-1-768x728.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 800px; --smush-placeholder-aspect-ratio: 800\/758;\" \/><\/a>\n<p>The draft amendments to the directives prepared by the European Commission were discussed in the European Parliament in autumn 2024. From January 2025 until early autumn, during the Polish and Danish Presidencies, a so-called trialogue took place between the Member States and the Council of the European Union, aimed at reaching a consensus on the legislative proposals for the amended water protection directives, including Directive 2008\/105\/EC. At the time of writing this article, the trialogue process had not yet been completed, but its conclusion was approaching. In the final stages of the trialogue, trifluoroacetic acid (TFA) was also included in the PFAS sum. It has been found that this perfluorinated organic compound, with the shortest hydrocarbon chain, also exhibits persistence in the environment [49]. TFA concentrations in surface waters vary widely, ranging from a few to several hundred ng\/l [50].<\/p>\n<p>Environmental quality standards are also proposed in the amendment to European Parliament and Council Directive 2006\/118\/EC on the protection of groundwater against pollution and deterioration. In light of the latest scientific knowledge, Annex\u202fI of this Directive is supplemented with a quality standard for the sum of the four most problematic PFAS (PFHxS, PFOS, PFOA, PFNA) and TFA, in accordance with the value proposed by the European Food Safety Authority (EFSA). To account for differences in the toxicity of the four PFAS and TFA, relative potency factors are applied when calculating the sum of these five substances. The EQS is also 0.0044\u202f\u00b5g\/l (4.4\u202fng\/l), the same as for surface water. The Directive notes that, in light of the latest scientific knowledge, it is important that the parameters for PFAS, including TFA, set out in Directive 2020\/2184\/EC be reviewed and, if necessary, revised in the near future, and that any such revisions be harmonised with the EQS set out in Annex\u202fI of Directive 2006\/118\/EC. Legislative approval of the amended directives is expected by the end of 2025.<\/p>\n<p>Within\u00a0the\u00a0EU, there is also an\u00a0ongoing intensive discussion on how to harmonise EQS for PFAS across surface water, groundwater, and water intended for human\u00a0consumption, which will be important for the\u00a0further development of\u00a0legislative instruments. It is also noted that the\u00a0current EQS cover only selected PFAS, even though many more (potentially several thousand) are present in\u00a0the\u00a0aquatic environment. For these reasons, the\u00a0European\u00a0Commission is preparing to establish EQS for the\u00a0total PFAS load in\u00a0surface waters. This is expected to take place during the\u00a0next review of\u00a0Directive 2008\/105\/EC. As part of\u00a0the\u00a0documentation for the\u00a0review, six proposals for addressing total PFAS have been prepared [51]. The\u00a0greatest consensus currently exists around the\u00a0proposal setting an\u00a0annual average EQS-RP of\u00a00.05\u202f\u00b5g\/l of\u00a0total organic fluorine for surface waters. The\u00a0Joint Research Centre (Italy) proposes measuring total organic fluorine, or \u201ctotal PFAS\u201d, only if the\u00a0corresponding EQS for the\u00a0sum of\u00a024 PFAS (for both surface waters and biota) has been met (not exceeded).<\/p>\n<p>The\u00a0relative potency factor (RPF) is used in\u00a0the\u00a0risk assessment of\u00a0mixtures of\u00a0perfluoroalkyl and polyfluoroalkyl substances to express their potential harmfulness relative to a\u00a0specific index compound, typically PFOA, for a\u00a0given health-relevant endpoint. By assigning an\u00a0RPF of\u00a01 to the\u00a0index compound, the\u00a0equivalent exposure of\u00a0any PFAS in\u00a0the\u00a0mixture can\u00a0be calculated as \u201cPFOA equivalents.\u201d This allows for a\u00a0more accurate assessment of\u00a0the\u00a0cumulative health risk posed by multiple PFAS, which often co-occur in\u00a0environmental contamination.<\/p>\n<p>The requirements of Directive 2008\/105\/EC, as amended by Directive 2013\/39\/EU, have been transposed into national legislation on the\u00a0protection of\u00a0surface waters through Government Regulation No\u202f401\/2015\u202fColl.\u202f[52]. Currently, environmental quality standards have been established only for PFOS, set at 6.5\u202f\u2219\u202f10<sup>-4<\/sup>\u202f\u00b5g\/l (annual average EQS) and 36\u202f\u00b5g\/l as the\u00a0maximum allowable concentration.<\/p>\n<p>The\u00a0amended Decree No.\u202f428\/2001\u202fColl.\u202f[53] already incorporates a\u00a0quality limit for raw surface water (intended for treatment to drinking water) for the\u00a0sum of\u00a020\u00a0PFAS in\u00a0accordance with European\u00a0Parliament and Council Directive 2020\/2184 (0.1\u202f\u00b5g\/l) for all three categories of\u00a0raw water treatment: A1, A2, and A3.<\/p>\n<h3>An overview of analytical methods for PFAS determination<\/h3>\n<p>A\u00a0range of\u00a0analytical methods has been developed for PFAS monitoring, enabling their determination at sub\u2011nanogram levels. Most methods employ liquid chromatography coupled with mass spectrometric detection. They mainly differ in\u00a0the\u00a0sample preparation approach \u2013 direct injection, online and offline solid-phase extraction (SPE), or dispersive magnetic solid-phase extraction (DMSPE) are all possible. The\u00a0method applied for analysing water at the\u00a0inlet and outlet of\u00a0a\u00a0drinking water treatment plant in\u00a0Catalonia is based on the\u00a0direct injection of\u00a0900\u202f\u00b5l of\u00a0sample without any prior preparation [54]. A\u00a0similar method, also based on the\u00a0direct injection of\u00a0100\u202f\u00b5l of\u00a0centrifuged water sample without any further preparation, using UHPLC\u2011MS\/MS for the\u00a0analysis of\u00a0several perfluoroalkyl acids (PFAA) across a\u00a0wide range of\u00a0water matrices, demonstrated high sensitivity (sub\u2011nanogram quantification), speed, accuracy, and low matrix effects [55]. A\u00a0direct injection method of\u00a0150\u202f\u00b5l of\u00a0water sample using an\u00a0Agilent\u202f1100\u00a0HPLC coupled to a\u00a0Waters Quattro Micro tandem mass spectrometer is described in\u00a0a\u00a0study analysing both water and soil samples [56]. Another analytical method applicable for the\u00a0determination of\u00a0these contaminants is based on solid-phase extraction (SPE) followed by gas chromatography with negative chemical ionisation and mass spectrometric detection. The\u00a0method is highly sensitive, and the\u00a0results are fully comparable with those obtained using HPLC\u2013MS\/MS. Using this method, surface water samples from the\u00a0Vltava and Elbe rivers were tested, and the\u00a0target substances were detected in\u00a0all samples [57]. A\u00a0further review study [58] is devoted to analytical methods for PFAS determination developed and applied between 2018 and 2023. For PFAS extraction, solid-phase extraction is most commonly used, followed primarily by liquid chromatography coupled with mass spectrometry for quantification [58]. A\u00a0solid-phase extraction method using 100\u202fml of\u00a0water sample was applied to determine 22 PFAS in\u00a0drinking water in\u00a0the\u00a0Czech Republic. High-performance liquid chromatography coupled with mass spectrometric detection was used for the\u00a0actual analysis. Using this method, 67 tap water samples and 31 bottled water samples were analysed. PFAS intake by an\u00a0adult from tap or bottled water amounted to a\u00a0few per cent of\u00a0the\u00a0tolerable weekly intake established by the\u00a0European\u00a0Food Safety Authority and therefore did not represent a\u00a0significant risk [59].<\/p>\n<p>Another direct injection method for the\u00a0analysis of\u00a0PFAS in\u00a0environmental water samples uses centrifugation and membrane filtration of\u00a0small sample volumes, which are then analysed by UHPLC\u2011ESI\u2011MS\/MS using a\u00a0delay column to reduce interference from background PFAS contamination. For the\u00a0actual analysis,<br \/>\nan\u00a0AB Sciex 6500\u202fplus Q\u2011Trap mass spectrometer is used, operated in\u00a0negative multiple reaction monitoring (MRM) mode. The\u00a0instrument system includes a\u00a0delay column positioned between the\u00a0pumps and the\u00a0autosampler to reduce interference from background PFAS. The\u00a0method monitors eight short\u2011 and long\u2011chain\u00a0PFAS, which are identified by tracking specific precursor\u2013product ion pairs and their retention times, and quantified using calibration curves based on isotopically labelled internal standards. The\u00a0method is technically robust and provides sufficient sensitivity and reproducibility for use as a\u00a0primary screening approach to detect and quantify PFAS at levels typically observed in\u00a0surface and drinking waters. It can\u00a0accurately detect and quantify common PFAS, including PFOA and PFOS, at concentrations below the\u00a0commonly recommended screening level of\u00a070\u202fng\/l [60].<\/p>\n<p>Another study [61] addresses the\u00a0determination of\u00a0PFAS in\u00a0accordance with Directive 2020\/2184\/EU using the\u00a0prescribed methods. In\u00a0this paper, three different methods were developed and evaluated for the\u00a0determination of\u00a020\u00a0PFAS in\u00a0tap and bottled water, based on online and offline solid-phase extraction (SPE) and direct injection. In\u00a0all cases, ultra\u2011high\u2011performance liquid chromatography coupled with tandem mass spectrometry (UHPLC\u2011MS\/MS) was used as the\u00a0analytical technique. Offline SPE using Oasis Weak Anion Exchange (WAX) cartridges provided the\u00a0best performance in\u00a0terms of\u00a0quantification limits (LOQ\u202f\u2264\u202f0.3\u202fng\/l) and accuracy (R\u202f\u2265\u202f70\u202f%) in\u00a0drinking water samples. Online SPE and direct injection had certain\u00a0drawbacks, such as background contamination issues and lower accuracy for the\u00a0least polar compounds. The\u00a0offline method was applied to the\u00a0analysis of\u00a046\u00a0drinking water samples, including 11\u00a0commercial bottled samples, 23 Spanish tap water samples, and 12 international tap water samples [61].<\/p>\n<p>In\u00a0Greece, a\u00a0method combining ultra-performance liquid chromatography (UPLC) with Orbitrap mass spectrometry (Orbitrap-MS), using an\u00a0electrospray ionisation (ESI) interface in\u00a0negative mode, was developed, validated and applied to real samples. Samples of\u00a0lake and seawater, as well as wastewater from municipal and hospital WWTPs, were analysed. The\u00a0concentrations in\u00a0surface waters were below the\u00a0limit of\u00a0detection or significantly lower than\u00a0those in\u00a0wastewater [62].<\/p>\n<p>Another emerging method aimed at accelerating and simplifying PFAS determination applies dispersive magnetic solid-phase extraction (DMSPE) to enrich PFAS in\u00a0various surface water samples. For the\u00a0preconcentration and extraction of\u00a0PFAS from various river water samples, magnetic Fe\u2083O\u2084 @ MIL-101 (Cr) was used for the\u00a0first time as an\u00a0adsorbent in\u00a0MSPE. Concentrations of\u00a0the\u00a0target analytes in\u00a0the\u00a0water samples were determined using high-performance liquid chromatography with a\u00a0diode-array detector and ultra-high-performance liquid chromatography \u2013 tandem mass spectrometry [63].<\/p>\n<p>To assess PFAS contamination levels in\u00a0sludge originating from selected PFAS at 43 WWTPs in\u00a0the\u00a0Czech Republic, an\u00a0analytical screening method was developed and validated for 32 PFAS representatives, including new substitutes (e.g.\u00a0GenX, sodium dodecafluoro-3H-4-oxanonanoate, 8-dioxanonanoate \u2013 NaDONA). For the\u00a0risk assessment of\u00a0agricultural use of\u00a0WWTP sludge commonly applied as fertiliser, human\u00a0exposure to PFAS was calculated for various types of\u00a0vegetables grown in\u00a0soil potentially fertilised with realistically contaminated sludge in\u00a0the\u00a0Czech Republic [64].<\/p>\n<p>A\u00a0method for the\u00a0quantitative determination of\u00a0PFOS was also developed using high-performance liquid chromatography (HPLC) coupled with Orbitrap mass spectrometry (Orbitrap-MS), employing a\u00a0heated electrospray ionisation (HESI) interface operated in\u00a0negative mode. HPLC separation of\u00a0the\u00a0analytes was achieved using a\u00a0reversed-phase C18 analytical column (RP-C18). The\u00a0method enables reliable monitoring of\u00a0PFOS and its derivatives in\u00a0environmental samples in\u00a0accordance with the\u00a0criteria of\u00a0the\u00a0environmental quality standard, taking into account the\u00a0maximum permissible concentrations and the\u00a0annual average concentrations specified in\u00a0Directive 2013\/39\/EU. The\u00a0method was applied for the\u00a0routine analysis of\u00a0selected PFAS in\u00a0environmental samples from the\u00a0Baltic Sea region [65].<\/p>\n<p>A non-target screening (NTS) approach based on high-resolution mass spectrometry (HRMS) is also essential for the comprehensive characterisation of PFAS in environmental, biological, and technical samples, due to the very limited availability of authentic PFAS reference standards. Since MS\/MS information is not always achievable in trace analysis and only selected PFAS are present within homologous\u00a0series, additional techniques for prioritising HRMS-measured data according to their probability of\u00a0being PFAS are highly desirable. The\u00a0procedure proposed in\u00a0the\u00a0study could also be applied to the\u00a0monitoring of\u00a0other groups of\u00a0compounds [66].<\/p>\n<p>Given the\u00a0approaching obligation to regularly monitor the\u00a0concentrations of\u00a0selected PFAS, methods enabling highly sensitive analysis for the\u00a0routine determination of\u00a0PFAS in\u00a0various types of\u00a0water (drinking water, surface water, and groundwater) are being developed rapidly [67, 68]. Simultaneously, methods for the\u00a0quantification of\u00a0short-chain\u00a0and ultra-short-chain\u00a0PFAS are being developed [69].<\/p>\n<p>Due to the\u00a0fact that there is a\u00a0very large number of\u00a0PFAS and it is rather demanding to identify or quantify all of\u00a0them in\u00a0a\u00a0sample, simpler methods for determining total organic fluorine are increasingly being adopted for screening purposes. The\u00a0most commonly used method for this purpose is the\u00a0determination of\u00a0adsorbable organic fluorine (AOF), which provides non-specific information on the\u00a0amount of\u00a0organofluorine compounds. A\u00a0procedure using combustion ion chromatography (CIC) covers a\u00a0wide range of\u00a0organofluorine compounds that are currently not detectable by LC-MS\/MS. AOF is important for estimating unknown PFAS concentrations, screening PFAS contamination, and assessing PFAS exposure [70, 71].<\/p>\n<p>As noted above, the\u00a0number of\u00a0publications addressing PFAS is enormous. The\u00a0main\u00a0challenges that must be addressed when analysing PFAS are high background levels, which require strictly followed procedures at the\u00a0very stage of\u00a0sample collection, and the\u00a0careful selection of\u00a0suitable sampling containers and other tools used during sample processing. Given the\u00a0very strict environmental quality standards proposed in\u00a0European\u00a0legislation, methods for determining PFAS are highly demanding in\u00a0terms of\u00a0instrumentation. Due to their widespread presence, background levels of\u00a0the\u00a0target compounds can\u00a0be high even in\u00a0standard laboratory equipment. Some components of\u00a0analytical instruments also need to be replaced with PFAS-free equivalents.<\/p>\n<h3 class=\"03NADPIS3\">Sampling<\/h3>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">Due to the\u00a0ubiquitous presence of\u00a0PFAS, even the\u00a0simple act of\u00a0sampling is complicated, including the\u00a0choice of\u00a0materials for the\u00a0sample containers. The\u00a0influence of\u00a0storage and sample preparation conditions \u2013 such as storage duration, solvent composition, storage temperature (4\u202f\u00b0C and 20\u202f\u00b0C), and sample mixing technique (shaking or centrifugation) \u2013 on PFAS losses into container materials was studied for commonly used HDPE materials, including polypropylene (PP), polystyrene (PS), polypropylene copolymer (PPCO), polyethylene terephthalate (PET), polytetrafluoroethylene (PTFE), and glass. The\u00a0highest losses of\u00a0long-chain\u00a0PFAS in\u00a0aqueous solutions were observed with polypropylene. Sorptive losses of\u00a0long-chain\u00a0PFAS decreased in\u00a0an\u00a080 : 20 water : methanol solution (%, v\/v). Sorption losses of\u00a0PFAS with temperature were dependent on the\u00a0solvent composition [72]. When sampling for these compounds, strict procedures must be followed to prevent secondary contamination. Sampling equipment and accessories must not contain\u00a0materials such as PTFE, PVDF, PCTFE, ETFE, or FEP (e.g., commercial brands Teflon\u00ae, Hostaflon\u00ae, Kynar\u00ae, Neoflon\u00ae, Tefzel\u00ae). LDPE must not be used in\u00a0direct contact with the\u00a0sample medium (e.g., for sample containers) but may be present in, e.g., protective bags. HDPE is most commonly used for sample containers and should be pre-tested for the\u00a0presence of\u00a0PFAS.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">Field clothing and footwear used by sampling personnel must not contain\u00a0Gore-Tex\u00ae or other waterproof\u00a0materials, nor materials with stain-repellent surface treatments. Suitable clothing and footwear include items made of\u00a0cotton, PVC, or polyurethane that have been repeatedly washed beforehand without synthetic softeners. PFAS may also be present in\u00a0a\u00a0wide range of\u00a0personal care products, including cosmetics, creams, shampoos, repellents, etc. Therefore, it is recommended not to apply such products on the\u00a0day of\u00a0sampling or during sampling activities, in\u00a0order to avoid any contact between these products and the\u00a0sampling equipment and materials. Provided that all other principles are observed, these products may be used before sampling work begins, but their application in\u00a0the\u00a0field during sampling (for example, sunscreens or insect repellents) should be avoided. The\u00a0basic precaution is thorough hand washing and the\u00a0use of\u00a0powder-free nitrile gloves.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">Sample contamination may also occur during transport. It is therefore essential to avoid all of\u00a0the\u00a0above-mentioned materials, water-repellent labels on sample containers, and permanent markers. To check for possible contamination during sampling and transport, field blanks and transport blanks are collected [73].<\/span><\/p>\n<h3 class=\"03NADPIS3\">Current monitoring of PFAS in surface waters in\u00a0the\u00a0Czech Republic<\/h3>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">Substances from the\u00a0PFAS group are not yet monitored systematically across the\u00a0entire Czech Republic. An\u00a0analysis was carried out of\u00a0the\u00a0available monitoring data for individual substances from this group obtained from the\u00a0river basin\u00a0authorities, which conducted monitoring of\u00a0surface water quality. When calculating average values (annual averages or overall averages for the\u00a0period during which PFAS compounds were monitored), values below the\u00a0limit of\u00a0quantification (LOQ) were included at the\u00a0LOQ level.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">In\u00a0the\u00a0<strong><span class=\"01BOLD\">Oh\u0159e river basin<\/span><\/strong>, PFOS was measured annually from 2012 to 2023 at\u00a042\u2013110\u00a0profiles. During 2012\u20132017, the\u00a0limit of\u00a0quantification (LOQ) was 0.010\u202f\u00b5g\/l, and from 2018 onward it was 0.020\u202f\u00b5g\/l. Throughout the\u00a0entire monitoring period, the\u00a0majority of\u00a0measurements were below the\u00a0LOQ, ranging from 70\u00a0% to 100\u00a0% in\u00a0individual years. Positive values therefore ranged from 0 % to 30\u00a0% in\u00a0individual years. Overall, 83 % of\u00a0measurements were below 0.020\u202f\u00b5g\/l, 16 % were between 0.020 and 0.100\u202f\u00b5g\/l, and 2 % exceeded 0.100\u202f\u00b5g\/l, with the\u00a0maximum recorded value reaching 0.600\u202f\u00b5g\/l. The\u00a0annual mean\u00a0values evaluated for the\u00a0entire basin\u00a0ranged from 0.010 to 0.021\u202f\u00b5g\/l in\u00a0individual years, with an\u00a0overall mean\u00a0of\u00a00.017\u202f\u00b5g\/l for the\u00a0entire period. In\u00a02024, monitoring of\u00a0PFAS in\u00a0the\u00a0Oh\u0159e basin\u00a0was initiated in\u00a0accordance with Directive 2020\/2184 on the\u00a0quality of\u00a0water intended for human\u00a0consumption in\u00a0drinking water reservoirs. The\u00a0LOQ used was 0.006\u202f\u00b5g\/l for PFBA and 0.001\u202f\u00b5g\/l for all other PFAS. Only a\u00a0few values above the\u00a0LOQ were detected for PFPeA, PFHxA, PFHpA, PFOA, PFDA, PFTrDA, PFBS, PFHpS, PFOS, PFDS, and PFTrDS, ranging from 0.001\u00a0to 0.014\u202f\u00b5g\/l.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">In\u00a0the\u00a0<strong><span class=\"01BOLD\">Odra river basin<\/span><\/strong>, only PFOS was measured at 80\u201382 river network profiles during 2017\u20132023, with a\u00a0LOQ of\u00a00.100\u202f\u00b5g\/l from 2017 to 2021, which was lowered to 0.010\u202f\u00b5g\/l in\u00a02022. Over the\u00a0entire monitoring period, only two positive values were recorded (0.210 and 0.400\u202f\u00b5g\/l in\u00a02018). Annual mean\u00a0values evaluated for the\u00a0whole basin\u00a0ranged from 0.010 to 0.101\u202f\u00b5g\/l, with a\u00a0mean\u00a0of\u00a00.075\u202f\u00b5g\/l for the\u00a0entire period.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">In\u00a0the\u00a0<strong><span class=\"01BOLD\">Morava river basin<\/span><\/strong>, PFOS and PFOA were monitored during 2013\u20132023 at 44\u2013100 profiles. The LOQ for PFOS was 0.020\u202f\u00b5g\/l in 2013\u20132019, 0.010\u202f\u00b5g\/l in 2020\u20132022, and 0.6\u202fng\/l from 2023. Throughout the entire evaluated period, values below LOQ predominated.\u00a0 The proportion of positive values in individual years up to 2022 was only 0\u20132\u202f%. Overall, 99.5 % of values were below 0.020\u202f\u00b5g\/l, 0.4 % were in the range 0.020\u20130.100\u202f\u00b5g\/l, 0.1 % were above 0.100\u202f\u00b5g\/l, and the maximum recorded value was 3.65\u202f\u00b5g\/l. Annual mean values calculated for the entire basin ranged from 0.0006 to 0.021\u202f\u00b5g\/l in individual years, with an overall average of 0.016\u202f\u00b5g\/l. Since 2023, when the LOQ was lowered to 0.6\u202fng\/l, approximately 10 % of results have exceeded the LOQ.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">For PFOA, the LOQ used throughout the entire period was 0.010\u202f\u00b5g\/l. Over the entire evaluated period, values below the LOQ predominated. In individual years up to 2022, only 0\u20132 % of values were positive. Overall, 99.6 % of values were below 0.010\u202f\u00b5g\/l, 0.3 % of values ranged from 0.010\u20130.100\u202f\u00b5g\/l, and 0.1 % of values were above 0.100\u202f\u00b5g\/l, with the maximum recorded value being 1.8\u202f\u00b5g\/l. Annual mean values, calculated for the entire catchment, ranged from 0.010\u20130.014\u202f\u00b5g\/l in individual years, with an overall mean of 0.011\u202f\u00b5g\/l. In 2024, monitoring of PFAS was initiated at 27 selected profiles in the Morava basin, covering the scope of Directive 2020\/2184 on the quality of water intended for human consumption and the proposed amendment to European Parliament and Council Directive 2008\/105\/EC. The applied LOQs for individual substances ranged from 0.018 to 1.0\u202fng\/l. In addition to PFOS and\u00a0<\/span><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">PFOA, PFBA, PFPeA, PFHxA, PFHpA, PFNA, PFDA, PFUnDA, PFBS, and PFHxS were also detected above the\u00a0LOQ, in\u00a0the\u00a0range of\u00a00.02\u201312.6\u202fng\/l.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">In\u00a0the\u00a0<strong><span class=\"01BOLD\">Elbe river basin<\/span><\/strong>, PFOS and PFOA were monitored annually from 2012 to 2024 at 20\u2013130 profiles. The LOQ for PFOS was 0.020\u202f\u00b5g\/l in 2012\u20132015, 0.002\u202f\u00b5g\/l in 2016\u20132017, and 1\u202fng\/l from 2018 onwards. Throughout the entire monitoring period, values below the LOQ predominated, accounting for approximately 70 % overall, with 96.5 % of values below 0.020\u202f\u00b5g\/l, 3.2 % ranging from 0.020 to 0.100\u202f\u00b5g\/l, 0.3 % exceeding 0.100\u202f\u00b5g\/l, and the maximum recorded value 0.568\u202f\u00b5g\/l. The annual mean values calculated for the entire basin ranged from 0.0013 to 0.031\u202f\u00b5g\/l in individual years, with a mean of 0.0054\u202f\u00b5g\/l for the entire period.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">For PFOA, the\u00a0LOQ was 0.020\u202f\u00b5g\/l in\u00a02012\u20132015, 0.005\u202f\u00b5g\/l in\u00a02016\u20132023, and 1\u202fng\/l from 2018 onwards. Throughout the\u00a0monitored period, values below the\u00a0LOQ predominated, accounting for about 95 %. Overall, 99.6 % of\u00a0the\u00a0values were below 0.020\u202f\u00b5g\/l, 0.4 % were in\u00a0the\u00a0range 0.020\u20130.100\u202f\u00b5g\/l, and the\u00a0maximum recorded value was 0.046\u202f\u00b5g\/l. Annual mean\u00a0values (evaluated for the\u00a0entire basin) ranged from 0.0025 to 0.020\u202f\u00b5g\/l in\u00a0individual years, with an\u00a0overall mean\u00a0of\u00a00.0063\u202f\u00b5g\/l. Broader PFAS monitoring in\u00a0this catchment started in\u00a02025.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">In\u00a0the\u00a0<strong><span class=\"01BOLD\">Vltava river basin<\/span><\/strong>, PFOS and PFOA were monitored on 28\u2013134 profiles during 2012\u20132024. The\u00a0LOQ for PFOS was 0.100\u202f\u00b5g\/l in\u00a02012\u20132013, 0.005\u202f\u00b5g\/l in\u00a02014\u20132021, 0.003\u202f\u00b5g\/l in\u00a02022, and 0.5\u202fng\/l from 2023 onwards. Throughout the\u00a0entire monitoring period, values below the\u00a0LOQ prevailed. Positive values in\u00a0individual years ranged from 0 % to 26 %. Overall, 87 % of\u00a0values were below 0.020\u202f\u00b5g\/l, 12.9 % were between 0.020 and 0.100\u202f\u00b5g\/l, 0.1 % were above 0.100\u202f\u00b5g\/l, and the\u00a0maximum recorded value was 0.289\u202f\u00b5g\/l. Annual mean\u00a0values evaluated for the\u00a0entire basin\u00a0ranged from 0.0022 to 0.100\u202f\u00b5g\/l in\u00a0individual years, with an\u00a0overall average of\u00a00.017\u202f\u00b5g\/l. Since 2023, when LOQ was lowered to 0.5\u202fng\/l, approximately 20 % of\u00a0results have exceeded the\u00a0LOQ.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.15pt;\">For PFOA, the\u00a0LOQ was 0.100\u202f\u00b5g\/l in\u00a02012\u20132013, 0.010\u202f\u00b5g\/l in\u00a02014\u20132021, 0.005\u202f\u00b5g\/l in\u00a02022, and 2\u202fng\/l from 2023 onwards. Throughout the\u00a0entire monitoring period, values below the\u00a0LOQ predominated. Positive values in\u00a0individual years ranged from only 0 % to 22 %. Overall, 87.4 % of\u00a0values were below 0.010\u202f\u00b5g\/l, 12.6 % were in\u00a0the\u00a0range 0.010\u20130.100\u202f\u00b5g\/l, and only a\u00a0single value exceeded 0.100\u202f\u00b5g\/l, with the\u00a0maximum recorded value being 0.111\u202f\u00b5g\/l. The\u00a0annual mean\u00a0values for the\u00a0entire basin\u00a0ranged from 0.0022 to 0.100\u202f\u00b5g\/l in\u00a0individual years, with an\u00a0overall mean\u00a0of\u00a00.020\u202f\u00b5g\/l. In\u00a02023, PFAS monitoring in\u00a0line with Directive 2020\/2184 on the\u00a0quality of\u00a0water intended for human\u00a0consumption was initiated at 42 selected profiles in\u00a0the\u00a0Vltava basin, and from 2024 it was extended to include four additional substances. The\u00a0applied LOQ for individual substances ranged from 0.5 to 6.0\u202fng\/l. In\u00a0addition to PFOS and PFOA, PFBA, PFBS, PFHxS, PFHpA, PFHxA, PFOS-H4, and PFTrDA were detected above the\u00a0LOQ in\u00a0the\u00a0range of\u00a01.2\u201355\u202fng\/l. Further details on the\u00a0monitoring of\u00a0these substances in\u00a0the\u00a0Vltava basin\u00a0are provided in\u00a0[74].<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.2pt;\">The values detected in surface waters in the Czech Republic can be compared with findings of PFAS compounds in other countries. Between 2004 and 2010, surface water samples from 41 cities across 15 countries were analysed. PFOS and PFOA were present in all samples, with average concentrations ranging from non-detectable (ND) to 0.070 \u00b5g\/l for PFOS and 0.0002\u20131.630 \u00b5g\/l for PFOA. The maximum average PFOS concentration in surface waters in the United Kingdom was 0.019 \u00b5g\/l. The PFOA concentration in surface waters in Osaka reached 1.630 \u00b5g\/l. In the other cities included in the study, average PFOA concentrations were generally below 0.100 \u00b5g\/l. In surface water from the J\u00facar River, PFAS were detected at concentrations ranging from 0.04 ng\/l to 0.0831 \u00b5g\/l. In Sweden, average concentrations of 26 PFAS were found in samples collected from drinking water source areas at 0.0084 \u00b5g\/l, in surface waters at 0.112 \u00b5g\/l, and in groundwater at 0.049 \u00b5g\/l. In surface waters of the Rhine river basin, from Lake Constance to the North Sea, the concentrations of 40 PFAS were examined to assess the impact of both point and diffuse sources. Among the PFAS, perfluorobutane sulfonic acid (PFBS) predominated with concentrations up to 0.181 \u00b5g\/l, and perfluorobutanoic acid (PFBA) with concentrations up to 0.335 \u00b5g\/l. These two compounds accounted for up to 94 % of the total PFAS [24].<\/span><\/p>\n<h3 class=\"03NADPIS3\">Pilot extension of monitoring to additional profiles<\/h3>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\">To supplement the\u00a0monitoring profiles of\u00a0PFAS substances on a\u00a0broader scale, pilot monitoring was proposed in\u00a0the\u00a0Oh\u0159e and Odra river basins. In\u00a0collaboration with the\u00a0river basin\u00a0administrators major closing profiles and sites with repeated PFOS detections above the\u00a0limit of\u00a0quantification were selected. These profiles are listed in\u00a0<em><span class=\"01ITALIC\">Tab. 2<\/span><\/em>. In\u00a0addition to the\u00a0sites in\u00a0the\u00a0target river basins, the\u00a0Kopaninsk\u00fd stream on the\u00a0outskirts of\u00a0Prague was included, as it is strongly affected by V\u00e1clav Havel Airport.<\/span><\/p>\n<h5>Tab.\u00a02. Selected sampling profiles<\/h5>\n<a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-2-1.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-37144 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-2-1.jpg\" alt=\"\" width=\"800\" height=\"900\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-2-1.jpg 800w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-2-1-267x300.jpg 267w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-2-1-768x864.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 800px; --smush-placeholder-aspect-ratio: 800\/900;\" \/><\/a>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\">A\u00a0summary of\u00a0the\u00a0monitoring sites in\u00a0the\u00a0Oh\u0159e basin\u00a0is shown in\u00a0<em><span class=\"01ITALIC\">Fig.\u00a01<\/span><\/em>, the\u00a0sites sampled in\u00a0the\u00a0Odra basin\u00a0are presented in\u00a0<em><span class=\"01ITALIC\">Fig.\u00a02<\/span><\/em>, and <em><span class=\"01ITALIC\">Fig.\u00a03<\/span><\/em> shows the\u00a0sampling site on the\u00a0Kopaninsk\u00fd stream.<\/span><\/p>\n<a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-1.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-36923 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-1.jpg\" alt=\"\" width=\"800\" height=\"475\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-1.jpg 800w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-1-300x178.jpg 300w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-1-768x456.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 800px; --smush-placeholder-aspect-ratio: 800\/475;\" \/><\/a>\n<h6>Fig. 1. Location map of\u00a0Oh\u0159e basin\u00a0profiles<\/h6>\n<h6><a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-2.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-36924 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-2.jpg\" alt=\"\" width=\"800\" height=\"506\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-2.jpg 800w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-2-300x190.jpg 300w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-2-768x486.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 800px; --smush-placeholder-aspect-ratio: 800\/506;\" \/><\/a><\/h6>\n<h6>Fig. 2. Location map of\u00a0Odra basin\u00a0profiles<\/h6>\n<h6><a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-3.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-36925 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-3.jpg\" alt=\"\" width=\"800\" height=\"504\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-3.jpg 800w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-3-300x189.jpg 300w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-obr-3-768x484.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 800px; --smush-placeholder-aspect-ratio: 800\/504;\" \/><\/a><\/h6>\n<h6>Fig. 3. Location of the sampling profile on the\u00a0Kopaninsk\u00fd stream<\/h6>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\">The\u00a0sampling also includes the\u00a0measurement of\u00a0field parameters: air temperature, water temperature, and water electrical conductivity. At profiles where it is possible, the\u00a0flow is recorded at the\u00a0nearest gauging station.<\/span><\/p>\n<h2 class=\"03NADPIS2\">ANALYTICAL METHODS USED FOR THE\u00a0DETERMINATION AND IDENTIFICATION OF\u00a0PFAS<\/h2>\n<h3 class=\"03NADPIS3\" style=\"margin-top: 0cm;\">Target analysis<\/h3>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\">In\u00a0developing the\u00a0method for determining PFAS in\u00a0surface water, we based our approach on published methods that employed similar instrumentation [67, 68]. A\u00a0liquid chromatography method with mass spectrometric detection under negative electrospray ionization conditions was selected. Methanolic standard solutions were purchased from Neochema and Altium International, as well as internal standards from Wellington Laboratories, and instrument accessories for PFAS analysis.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\">Analyses were carried out on an\u00a0Exion LC\/SCIEX liquid chromatograph coupled with a\u00a0Triple Quad\u2122 7500 mass spectrometer using negative-mode electrospray ionization, Q<span class=\"01DOLNIINDEX\">0<\/span>D optimization, and simple mode for the\u00a0analysis. For analyte separation, a\u00a0delay column Phenomenex Luna Omega C18, 100\u00a0\u00c5, 50\u00a0\u00d7\u00a02.1\u00a0mm, 1.6 \u00b5m, and an\u00a0analytical column Phenomenex Luna Omega PS\u00a0C18, 100\u00a0\u00c5, 100\u00a0\u00d7\u00a03.0 mm, 3 \u00b5m, were used. For the\u00a0gradient elution of\u00a0analytes, mobile phase A\u00a0(20 mM ammonium acetate in\u00a0water) and mobile phase\u00a0B (methanol) were used. The\u00a0mobile phase flow rate was 0.6 ml\/min. The\u00a0initial concentration of\u00a0mobile phase A\u00a0was 90 %, decreasing to 45 % at 0.1 min. From 4.50 min\u00a0to 4.95\u00a0min, the\u00a0concentration of\u00a0mobile phase A\u00a0was 1 %, returning to 90 % at 5.0\u00a0min. This gradient was used for PFAS with shorter chains.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\">Long-chain\u00a0PFAS such as PFHxDA and PFODA are more hydrophobic than\u00a0short-chain\u00a0PFAS and appear to bind to polypropylene containers when the\u00a0methanol concentration is below 40 %. For these compounds, the\u00a0method had to be adjusted, and the\u00a0gradient elution conditions were modified. The\u00a0initial concentration of\u00a0mobile phase A\u00a0was 90 %, decreasing to 35 % at 1.5 min. At\u00a08\u00a0min, the\u00a0concentration of\u00a0phase A\u00a0was 5 %. From 8.1 min\u00a0to 12.0 min, the\u00a0concentration of\u00a0mobile phase A\u00a0was 1 %, rising to 90 % at 12.5 min. Calibration with the\u00a0internal standard was prepared over the\u00a0range 1\u2013200 ng\/l.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\">Sample preparation is performed as follows: 1 ml of the water sample is added to a 2 ml glass vial containing 0.65 ml of a mixed methanolic solution of surrogate standards (resulting in a concentration of 50 ng\/l for each standard). The final MeOH concentration in the diluted sample is 40 %, and standards, blanks, and control samples are prepared with the same methanol concentration. The volume of sample injected is 100 \u00b5\/l.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\">Optimal chromatographic conditions were tuned for each individual PFAS. For each analyte, two characteristic transitions are monitored, one of\u00a0which is for the\u00a0internal standard. <em><span class=\"01ITALIC\">Tab. 3<\/span><\/em> provides an\u00a0overview and characteristics of\u00a0the\u00a0internal standards assigned to each analyte. The\u00a0measured MRM transitions are listed in\u00a0<em><span class=\"01ITALIC\">Tab. 4<\/span><\/em>. The\u00a0method is ready for testing with analytical standards.<\/span><\/p>\n<h5>Tab. 3. Internal standards<\/h5>\n<a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-3-1.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-37145 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-3-1.jpg\" alt=\"\" width=\"800\" height=\"1524\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-3-1.jpg 800w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-3-1-157x300.jpg 157w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-3-1-538x1024.jpg 538w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-3-1-768x1463.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 800px; --smush-placeholder-aspect-ratio: 800\/1524;\" \/><\/a>\n<h5>Tab. 4. Selected diagnostic ions<\/h5>\n<a href=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-4-1-scaled.jpg\" rel=\"shadowbox[sbpost-37174];player=img;\"><img decoding=\"async\" class=\"alignnone wp-image-37146 size-full lazyload\" data-src=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-4-1-scaled.jpg\" alt=\"\" width=\"509\" height=\"2560\" data-srcset=\"https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-4-1-scaled.jpg 509w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-4-1-768x3862.jpg 768w, https:\/\/www.vtei.cz\/wp-content\/uploads\/2025\/12\/maresova-tab-4-1-407x2048.jpg 407w\" data-sizes=\"(max-width: 509px) 100vw, 509px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 509px; --smush-placeholder-aspect-ratio: 509\/2560;\" \/><\/a>\n<p class=\"03NADPIS3\">Non-target analysis<\/p>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\">For the\u00a0development of\u00a0a\u00a0non-targeted analysis method focused on PFAS, high-resolution liquid chromatography coupled with mass spectrometry and electrospray ionization in\u00a0negative mode was chosen.<\/span><\/p>\n<p class=\"00TEXTenglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.2pt;\">Analyses were performed on an\u00a0Agilent 1290 Infinity II liquid chromatograph coupled with a\u00a0SCIEX X500R QTOF mass spectrometer with electrospray ionization in\u00a0negative mode. In\u00a0the\u00a0first phase, a\u00a0universal method for non-targeted analysis using ammonium formate as the\u00a0mobile phase was tested. For PFAS, ammonium acetate was ultimately chosen as the\u00a0mobile phase. For the\u00a0separation of\u00a0analytes, an\u00a0Arion Plus C18 analytical column (100\u00a0\u00d7\u00a02.1\u00a0mm, 3\u00a0\u00b5m) was used. Mobile phase A\u00a0is 5\u00a0mM ammonium acetate, and mobile phase B is methanol. The\u00a0gradient starts at 95\u00a0% A\u00a0for 0.5\u202fmin\u00a0and decreases to 5 % A\u00a0by 14\u202fmin, where it is held for 4\u202fmin. At 18.1\u202fmin, the\u00a0concentration of\u00a0A\u00a0is raised back to 95 %. From 18.1\u202fmin\u00a0to 22\u202fmin, the\u00a0concentration of\u00a0A\u00a0is maintained at 95 %. The\u00a0column temperature is 30\u202f\u00b0C, and the\u00a0mobile phase flow rate is 0.2\u202fml\/min. The\u00a0injection volume is 100\u202f\u00b5l. Compounds are analysed using electrospray ionisation in\u00a0negative mode (ESI<sup>&#8211;<\/sup>) combining a\u00a0full scan\u00a0over the\u00a0mass range 70\u20131 200\u202fDa with data-independent acquisition. The\u00a0spray voltage is \u22124,500\u202fV, the\u00a0collision energy \u221235\u202fV, and the\u00a0declustering potential \u221280\u202fV\u00a0for all compounds. Compound identification is performed using a\u00a0spectral library.<\/span><\/p>\n<p class=\"03NADPIS2\">DISCUSSION AND CONCLUSIONS<\/p>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\" style=\"letter-spacing: -.2pt;\">Per- and polyfluoroalkyl substances (PFAS) are currently receiving considerable attention. These substances, due to their chemical properties, widespread use across various industrial sectors, environmental persistence, long-term bioaccumulation potential, and the\u00a0associated risks to human\u00a0health, raise significant concern. The\u00a0article summarizes the\u00a0legislative requirements for monitoring PFAS in\u00a0the\u00a0EU and the\u00a0Czech Republic, including the\u00a0lists of\u00a0substances according to European\u00a0Parliament and Council Directive 2020\/2184 and the\u00a0proposed amendment to Directive 2008\/105\/EC. Based on data provided by the\u00a0individual River Basin\u00a0Authorities, an\u00a0analysis of\u00a0the\u00a0current status of\u00a0PFAS monitoring in\u00a0surface waters in\u00a0the\u00a0Czech Republic was carried out. The\u00a0determination of\u00a0these substances is analytically demanding and requires the\u00a0implementation of\u00a0new methodologies, including instrumental equipment. In\u00a0the\u00a0individual river basins, these substances are monitored to varying extents and with differing sensitivity. Until 2022, only PFOS, as well as PFOA (except for the\u00a0Odra and Oh\u0159e basins) were systematically monitored in\u00a0surface waters in\u00a0the\u00a0Czech Republic. However, due to the\u00a0different LOQ used in\u00a0individual river basins in\u00a0previous years, when most results were lower than\u00a0the\u00a0stated LOQ, the\u00a0nature of\u00a0the\u00a0data does not allow for an\u00a0objective assessment of\u00a0the\u00a0situation throughout the\u00a0Czech Republic. With the\u00a0expansion of\u00a0analytical capabilities, methods are gradually being introduced that enable the\u00a0determination of\u00a0individual compounds with higher sensitivity and, in\u00a0particular, a\u00a0wider range of\u00a0PFAS substances monitored. Since 2023, monitoring of\u00a0PFAS has also started in\u00a0individual river basins in\u00a0accordance with the\u00a0requirements of\u00a0Directive 2020\/2184 on the\u00a0quality of\u00a0water intended for human\u00a0consumption and, where applicable, in\u00a0accordance with the\u00a0proposed amendment to Directive 2008\/105\/EC of\u00a0the\u00a0European\u00a0Parliament and of\u00a0the\u00a0Council, including the\u00a0pilot monitoring by TGM WRI described in\u00a0the\u00a0article. Following the\u00a0final approval of\u00a0the\u00a0amendment to Directive 2008\/105\/EC, there will be a\u00a0need to transpose the\u00a0new environmental quality standards for PFAS into Government Regulation No. 401\/2015 Coll. According to the\u00a0latest status of\u00a0the\u00a0discussions (in\u00a0September 2025), the\u00a0transposition deadline is expected to be 21\u00a0December 2027. By the\u00a0same date, Member States shall establish a\u00a0supplementary monitoring program for PFAS (including other newly identified priority substances) and, by 22\u00a0December 2030, a\u00a0preliminary programme of\u00a0measures concerning these substances.<\/span><\/p>\n<h3 class=\"03NADPIS3literaturapodekovaniautori\">Acknowledgements<\/h3>\n<p class=\"00TEXTbezodsazenienglish\"><em><span class=\"01ITALIC\"><span lang=\"EN-GB\" style=\"letter-spacing: -.1pt;\">This study was conducted as part of\u00a0Project no. SS07010208 Research on the\u00a0Identification and Quantification of\u00a0Selected PFAS in\u00a0Surface Waters (PFAS-SW), funded by the\u00a0Technology Agency of\u00a0the\u00a0Czech Republic (TA CR) under the\u00a0Programme of\u00a0Applied Research, Experimental Development, and Innovations in\u00a0the\u00a0Field of\u00a0the\u00a0Environment\u00a0\u2013 Environment for Life, Subprogramme 1\u00a0\u2013 Operational Research in\u00a0the\u00a0Public Interest. Important information for the\u00a0project was provided by the\u00a0cooperating state enterprises Oh\u0159e Basin, Odra Basin, Vltava Basin, Elbe Basin, and Morava Basin\u00a0Authorities.<\/span><\/span><\/em><\/p>\n<p class=\"00TEXTbezodsazenienglish\"><span lang=\"EN-GB\">The\u00a0Czech version of\u00a0this article was peer-reviewed, the\u00a0English version was translated from the\u00a0Czech original by Environmental Translation Ltd.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Per- and polyfluorinated compounds (PFAS), a group of fluorinated compounds of anthropogenic origin, have been classified as a persistent organic substances of significant concern due to their chemical properties, widespread use in a number of industrial sectors, environmental spread, long term bioaccumulation potential, and resulting risk to human health. This article brings an overview of current knowledge about the occurrence of PFAS in the environment, mainly in surface, ground, and drinking water and about the methods of their removal from con-taminated water. Furthermore, the legislative requirements regarding PFAS at the level of the EU and Czech Republic are summarised here, including the list of compounds according to the Directive of the European Parliament and the Council 2020\/2184 and the Proposal for a Directive of the European Parliament and the Council 2008\/105\/EC.<\/p>\n","protected":false},"author":8,"featured_media":37088,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[2,87,92],"tags":[1511,3961,3989,3326,316,3988],"coauthors":[327,599,493,1855,239,1857,1848],"class_list":["post-37174","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-from-the-world-of-water-management","category-hydrochemistry-radioecology-microbiology","category-main","tag-czech-republic","tag-hplc-ms","tag-non-target-analysis","tag-pfas","tag-surface-water","tag-target-analysis"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/posts\/37174","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/comments?post=37174"}],"version-history":[{"count":9,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/posts\/37174\/revisions"}],"predecessor-version":[{"id":37600,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/posts\/37174\/revisions\/37600"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/media\/37088"}],"wp:attachment":[{"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/media?parent=37174"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/categories?post=37174"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/tags?post=37174"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/www.vtei.cz\/en\/wp-json\/wp\/v2\/coauthors?post=37174"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}