RESUMEN
Plastic contamination is widely recognized as a major environmental concern due to the entry of small plastic particles into the food chain, thereby posing potential hazards to human health. However, the current understanding of microplastic (MP; < 5 mm) particles in livestock, which serve as an important food source, is limited. This study aims to investigate the concentration and characteristics of MPs in edible tissues of cow and sheep, namely liver, meat, and tripe, obtained from butcher shops in five areas of Bushehr port, Iran. The mean concentration of MPs in different tissues of cow and sheep were 0.14 and 0.13 items/g, respectively. Among the examined tissues, cow meat exhibited the highest concentration of MPs, with a concentration of 0.19 items/g. Nylon and fiber were identified as the predominant polymer types and shapes of MPs found in cow and sheep tissues, respectively. Furthermore, no statistically significant difference was observed in MP concentration across different tissues of cow and sheep. Significantly, this study highlights the elevated hazards associated with exposure to MPs through the consumption of edible cow and sheep tissues, particularly for children who consume meat. The results underscore the potential transfer of MPs from the environment to livestock bodies through their food, contamination during meat processing, and subsequent health hazards for consumers.
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Microplásticos , Plásticos , Niño , Animales , Bovinos , Ovinos , Humanos , Ganado , Carne , HígadoRESUMEN
Urban runoff seems an obvious pathway for the transfer of microplastics (MPs) and phthalate acid esters (PAEs) from land-based sources to the marine environment; an issue that still lacks attention. This study presents the first results on MP and PAE levels in the urban runoff into the northern part of the Persian Gulf during the dry season. Average concentrations of MPs and PAEs in the urban runoff of eight selected sampling sites (N = 72) along the Bushehr coast were 1.86 items/L and 53.57 µg/L, respectively. MPs with a size range of 500-1000 µm had the highest abundance, and the mean levels of PAEs in MPs were 99.77 µg/g. The results of this study show that urban runoff is a main source of MP and PAE contaminants that are discharged into the Persian Gulf. Therefore, to decrease these pollutants from entering the aquatic environment, decision-makers in the area should consider this problem and stop the direct discharging of urban runoff into water bodies.
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Ácidos Ftálicos , Contaminantes Químicos del Agua , China , Monitoreo del Ambiente , Ésteres , Océano Índico , Microplásticos , Ácidos Ftálicos/análisis , Plásticos , Contaminantes Químicos del Agua/análisisRESUMEN
Incineration of sewage sludge produces every year huge amounts of sewage sludge ash. Due to its porosity and composition, sewage sludge ash can be used as an adsorbent for heavy metal ions removal. The present paper discusses the efficiency and feasibility of its use as an adsorbent for Pb (II) and Cu (II) removal in single and binary systems. Sewage sludge ash dosage, pH influence, equilibrium and kinetic studies were examined. The results show that sewage sludge ash is an effective and environmentally friendly adsorbent. The maximum adsorption capacity was 25.0 mg/g for Pb (II) and 7.5 mg/g for Cu (II). The presence of the competitive metal led to lower adsorption rate. The study concludes that sewage sludge ash is a promising adsorbent for Pb (II) and Cu (II) removal from wastewater presenting both economic and environmental benefits.
Asunto(s)
Cobre/química , Plomo/química , Aguas del Alcantarillado , Purificación del Agua/métodos , Adsorción , Concentración de Iones de Hidrógeno , Iones , Cinética , Metales Pesados , Microscopía Electrónica de Rastreo , Aguas Residuales , Contaminantes Químicos del Agua/análisis , Difracción de Rayos XRESUMEN
Health risk and burden of disease induced by exposure to trihalomethanes (THMs, four compounds) and haloacetic acids (HAAs, 5 compounds) from drinking water through ingestion, dermal absorption, and inhalation routes were assessed based on one-year water quality monitoring in four urban communities (Bandar Deylam, Borazjan, Bushehr, and Choghadak) of Bushehr Province, Iran. The total average concentrations of THMs and HAAs at all the communities level were determined to be 92.9 ± 43.7 and 70.6 ± 26.5 µg/L, respectively. The dominant components of the THMs and HAAs were determined to be tribromomethane (TBM, 41.6%) and monobromoacetic acid (MBAA, 60.8%), respectively. The average contributions of ingestion, dermal absorption, and inhalation routes in exposure to the chlorination by-products (CBPs) were respectively 65.0, 15.4, and 19.6%. The total average non-carcinogenic risk as the hazard index (HI) and incremental lifetime cancer risk (ILCR) of the CBPs at all the communities level were found to be 4.03 × 10-1 and 3.16 × 10-4, respectively. The total attributable deaths, death rate (per 100,000 people), age-weighted disability-adjusted life years (DALYs), and age-weighted DALY rate for all ages both sexes combined at all the communities level were estimated to be 1.0 (uncertainty interval: UI 95% 0.3 to 2.8), 0.27 (0.08-0.75), 30.8 (11.3-100.1), and 8.1 (3.0-26.4), respectively. The average contribution of mortality (years of life lost due to premature mortality: YLLs) in the attributable burden of disease was 94.7% (94.4-95.6). Although in most of cases the average levels of the CBPs were in the permissible range of Iranian standards for drinking water quality, the average values of ILCRs as well as attributable burden of disease were not acceptable (the ILCRs were higher than the boundary limit of 10-5); therefore, implementation of interventions for reducing exposure to CBPs through drinking water especially in Kowsar Dam Water Treatment Plant is strictly recommended.
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Agua Potable , Trihalometanos , Contaminantes Químicos del Agua , Purificación del Agua , Desinfección , Femenino , Humanos , Irán , Masculino , Medición de Riesgo , Trihalometanos/toxicidad , Contaminantes Químicos del Agua/toxicidadRESUMEN
The main aim of this work is to substantiate the mechanism of 1-propanol oxidation by ozone in aqueous solution when the substrate is present in large excess. Further goals are assessment of the products, their formation yields as well as the kinetic parameters of the considered reaction. The reaction of ozone with 1-propanol in aqueous solution occurs via hydride transfer, H-abstraction and insertion. Of these three mechanisms, the largest share is for hydride transfer. This implies the extraction of an hydride ion from the activated C-H group by O3 according to reaction: (C2H5)(H)(HO)C-H + O3 â [(C2H5)(H)(HO)C+ + HO3-]cage â (C2H5)(H)(HO)C+ + HO3-. The experimentally determined products and their overall formation yields with respect to ozone are: propionaldehyde-(60 ± 3)%, propionic acid-(27.4 ± 1.0)%, acetaldehyde-(4.9 ± 0.3)%, acetic acid-(0.3 ± 0.1)%, formaldehyde-(1.0 ± 0.1)%, formic acid-(4.6 ± 0.3)%, hydrogen peroxide-(11.1 ± 0.3)% and hydroxyl radical-(9.8 ± 0.3)%. The reaction of ozone with 1-propanol in aqueous media follows a second order kinetics with a reaction rate constant of (0.64 ± 0.02) M-1·s-1 at pH = 7 and 23 °C. The dependence of the second order rate constant on temperature is described by the equation: l n k I I = ( 27.17 ± 0.38 ) - ( 8180 ± 120 ) × T - 1 , which gives the activation energy, Ea = (68 ± 1) kJ mol-1 and pre-exponential factor, A = (6.3 ± 2.4) × 1011 M-1 s-1. The nature of products, their yields and the kinetic data can be used in water treatment. The fact that the hydride transfer is the main pathway in the 1-propanol/ozone system can probably be transferred on other systems in which the substrate is characterized by C-H active sites only.
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1-Propanol/química , Ozono/química , Ácidos/química , Aldehídos/metabolismo , Peróxido de Hidrógeno/química , Radical Hidroxilo/química , Cinética , Modelos Químicos , Agua/químicaRESUMEN
This paper deals with reactions occurring in the aqueous system of 2-propanol/ozone. The considered reactions are discussed from thermodynamic and kinetic points of view. The major finding refers to the fact that 2-propanol reacts with O3 mainly via hydride transfer: (HO)(H3C)2CH + O3 â [(HO)(H3C)2C+ + HO3-]cage â (HO)(H3C)2C+ + HO3- â (H3C)2CO + H2O + O2 Arguments supporting this proposed mechanism are: high exergonicity of reaction (ΔG = -234 kJ mol-1 for the first two steps), low HO yield - (2.4 ± 0.5)% and high acetone yield - (87.2 ± 1.5)%. Other oxidation products detected within the system are acetaldehyde - (1.4 ± 0.1)%, formaldehyde - (4.0 ± 0.1)%, acetic acid - (2.8 ± 0.2)%, formic acid - (0.6 ± 0.2)% and hydrogen peroxide - (1.5 ± 0.1)%. The temperature dependence of the second order rate constant for the reaction 2-propanol + O3 â products is ln kII = 29.64-8500 × T-1. The activation energy and pre-exponential factor derived from this relationship are (71 ± 3) kJ mol-1 and (7.5 ± 6.4) × 1012 M-1 s-1, respectively. At 23 °C, the second order rate constant is kII = (2.7 ± 0.1) M-1 s-1. The low reaction rate can be explained by the transfer of one hydride ion from 2-propanol to electrophilic ozone.
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2-Propanol/química , Ozono/química , Acetona/química , Formiatos/química , Peróxido de Hidrógeno/química , Cinética , Oxidación-Reducción , Temperatura , Termodinámica , AguaRESUMEN
Pyridine, pyridazine, pyrimidine and pyrazine were investigated in their reaction with ozone. These compounds are archetypes for heterocyclic aromatic amines, a structural unit that is often present in pharmaceuticals, pesticides and dyestuffs (e.g., enoxacin, pyrazineamide or pyrimethamine). The investigated target compounds react with ozone with rate constants ranging from 0.37 to 57 M(-1) s(-1), hampering their degradation during ozonation. In OH radical scavenged systems the reaction of ozone with pyridine and pyridazine is characterized by high transformation (per ozone consumed) of 55 and 54%, respectively. In non scavenged system the transformation drops to 52 and 12%, respectively. However, in the reaction of pyrimidine and pyrazine with ozone this is reversed. Here, in an OH radical scavenged system the compound transformation is much lower (2.1 and 14%, respectively) than in non scavenged one (22 and 25%, respectively). This is confirmed by corresponding high N-oxide formation in the ozonation of pyridine and pyridazine, but probably low formation in the reaction of pyrimidine and pyrazine with ozone. With respect to reaction mechanisms, it is suggested that ozone adduct formation at nitrogen is the primary step in the ozonation of pyridine and pyridazine. On the contrary, ozone adduct formation to the aromatic ring seems to occur especially in the ozonation of pyrimidine as inferred from hydrogen peroxide yield. However, also OH radical reactions are supposed processes in the case of pyrimidine and in particular for pyrazine, albeit negligible OH radical yields are obtained. The low compound transformation in OH radical scavenged system can prove this. As a result of negligible OH radical yields in all cases (less than 6%) electron transfer as primary reaction pathway plays a subordinate role.
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Ozono/química , Piridinas , Peróxido de Hidrógeno/química , Cinética , Contaminantes Químicos del Agua/químicaRESUMEN
Anilines as archetypes for aromatic amines, which play an important role in the production of, e.g., dyestuffs, plastics, pesticides or pharmaceuticals were investigated in their reaction with ozone. Due to their high reactivity towards ozone (1.2 × 10(5)-2.4 × 10(6) M(-1) s(-1)) the investigated aniline bearing different substituents are readily degraded in ozonation. However, around 4 to 5 molecules of ozone are needed to yield a successful transformation of aniline, most likely due to a chain reaction that decomposes ozone without compound degradation. This is inferred from OH radical scavenging experiments, in which compound transformation per ozone consumed is increased. Mechanistic considerations based on product formation indicate that addition to the aromatic ring is the preferential reaction in the case of aniline, p-chloroaniline and p-nitroaniline (high amounts of o-hydroxyaniline, p-hydroxyaniline, chloride, nitrite and nitrate, respectively were found). For aniline an addition to the nitrogen happens but to a small extent, since nitroso- and nitrobenzene were observed as well. In the case of N-methylaniline and N,N-dimethylaniline, an electron transfer reaction from nitrogen to ozone was proven due to the formation of formaldehyde. In contrast, for p-methylaniline and p-methoxyaniline the formation of formaldehyde may result from an electron transfer reaction at the aromatic ring. Additional oxidation pathways for all of the anilines under study are reactions of hydroxyl radicals formed in the electron transfer of ozone with the anilines (OH radical yields = 34-59%). These reactions may form aminyl radicals which in the case of aniline can terminate in bimolecular reactions with other compounds such as the determined o-hydroxyaniline by yielding the detected 2-amino-5-anilino-benzochinon-anil.
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Compuestos de Anilina , Ozono , Radical Hidroxilo , Cinética , Oxidación-ReducciónRESUMEN
Piperidine, piperazine and morpholine as archetypes for secondary heterocyclic amines, a structural unit that is often present in pharmaceuticals (e.g., ritalin, cetirizine, timolol, ciprofloxacin) were investigated in their reaction with ozone. In principle the investigated compounds can be degraded with ozone in a reasonable time, based on their high reaction rate constants with respect to ozone (1.9 × 10(4)-2.4 × 10(5) M(-1) s(-1)). However, transformation is insufficient (13-16%), most likely due to a chain reaction, which decomposes ozone. This conclusion is based on OH scavenging experiments, leading to increased compound transformation (18-27%). The investigated target compounds are similar in their kinetic and stoichiometric characteristics. However, the mechanistic considerations based on product formation indicate various reaction pathways. Piperidine reacts with ozone via a nonradical addition reaction to N-hydroxypiperidine (yield: 92% with and 94% without scavenging, with respect to compound transformation). However, piperazine degradation with ozone does not lead to N-hydroxypiperazine. In the morpholine/ozone reaction, N-hydroxymorpholine was identified. Additional oxidation pathways in all cases involved the formation of OH with high yields. One important pathway of piperazine and morpholine by ozonation could be the formation of C-centered radicals after ozone or OH radical attack. Subsequently, O2 addition forms unstable peroxyl radicals, which in one pathway loose superoxide radicals by generating a carbon-centered cation. Subsequent hydrolysis of the carbon-centered cation leads to formaldehyde, whereby ozonation of the N-hydroxy products can proceed in the same way and in addition give rise to hydroxylamine. A second pathway of the short-lived peroxyl radicals could be a dimerization to form short-lived tetraoxides, which cleave by forming hydrogen peroxide. All three products have been found.