Understanding how engineered nanoparticles (ENPs) interact with natural organic acids is important to ecological risk assessment of ENPs, but this interaction remains poorly studied. Here, we investigate the dispersion stability, ion release, and toxicity of yttrium oxide nanoparticles (nY2O3) suspensions after exposure to two low molecular weight natural organic acids (LOAs), namely benzoic acid and gallic acid. We find that in the presence of LOAs the nY2O3 suspensions become more stable with surface zeta potential more positive or negative, accompanied by small agglomerated size. LOA interaction with nY2O3 is shown to promote the release of dissolved yttrium from the nanoparticles, depending on the concentrations of LOAs. Toxic effects of the nY2O3 suspensions incubated with LOAs on Scenedesmus obliquus as a function of their mixture levels show three types of signs: stimulation, inhibition, and alleviation. The mechanism of the effects of LOAs on the nY2O3 toxicity may be mainly associated with the degree of agglomeration, particle-induced oxidative stress, and dissolved yttrium. Our results stressed the importance of LOA impacts on the fate and toxicity of ENPs in the aquatic environment.

Arsenic (As) is a highly toxic metalloid adversely affecting the environment, human health, and crop productivity. The present study assessed the synergistic effects of salinity and As on photosynthetic attributes, stomatal regulations, and metabolomics responses of the xero-halophyte Salvadora persica to decipher the As-salinity cross-tolerance mechanisms and to identify the potential metabolites/metabolic pathways involved in cross-tolerance of As with salinity. Salinity and As stress-induced significant stomatal closure in S. persica suggests an adaptive response to decrease water loss through transpiration. NaCl supplementation improved the net photosynthetic rate (by +39%), stomatal conductance (by +190%), water use efficiency (by +55%), photochemical quenching (by +37%), and electron transfer rate (54%) under As stress as compared to solitary As treatment. Our results imply that both stomatal and non-stomatal factors account for a reduction in photosynthesis under high salinity and As stress conditions. A total of 64 metabolites were identified in S. persica under salinity and/or As stress, and up-regulation of various metabolites support early As-salinity stress tolerance in S. persica by improving antioxidative defense and ROS detoxification. The primary metabolites such as polyphenols (caffeic acid, catechin, gallic acid, coumaric acid, rosmarinic acid, and cinnamic acid), amino acids (glutamic acid, cysteine, glycine, lysine, phenylalanine, and tyrosine), citrate cycle intermediates (malic acid, oxalic acid, and α-ketoglutaric acid), and most of the phytohormones accumulated at higher levels under combined treatment of As + NaCl compared to solitary treatment of As. Moreover, exogenous salinity increased glutamate, glycine, and cysteine, which may induce higher synthesis of GSH-PCs in S. persica. The metabolic pathways that were significantly affected in response to salinity and/or As include inositol phosphate metabolism, citrate cycle, glyoxylate and dicarboxylate metabolism, amino acid metabolism, and glutathione metabolism. Our findings indicate that inflections of various metabolites and metabolic pathways facilitate S. persica to withstand and grow optimally even under high salinity and As conditions. Moreover, the addition of salt enhanced the arsenic tolerance proficiency of this halophyte.

The objective of present study was to obtain the fixation of nano zero valent iron (nZVI) particles on a permeable matrix and evaluate the performance of this composite material for the removal of Cr(VI) from contaminated waters. The experiments were carried out using the cationic resin Dowex 50WX2 as porous support of the iron nanoparticles. The work was carried out in two phases. The first phase involved the fixation of nZVI on the resin matrix. The resin granules were initially mixed with a FeCl3 solution to obtain the adsorption of Fe(III). Then the Fe(III) loaded resin (RFe) was treated with polyphenol solutions to obtain the reduction of Fe(III) to the elemental state. Two polyphenol solutions were tested as reductants, i.e. green tea extract and gallic acid. Green tea was found to be inefficient, probably due to the relatively big size of the contained polyphenol molecules, but gallic acid molecules were able to reach adsorbed Fe(III) and reduce the cations to the elemental state. The second phase was focused on the investigation of Cr(VI) reduction kinetics using the nanoiron loaded resins (R-nFe). It was found that the reduction follows a kinetic law of first order with respect to Cr(VI) and to the embedded nanoiron. Compared to other similar products, this composite material was found to have comparable performance regarding reaction rates and higher degree of iron utilization. Namely the rate constant for the reduction of Cr(VI), in the presence of 1 mM nZVI, was equivalent to 1.4 h of half-life time at pH 3.2 and increased to 24 h at pH 8.5. The degree of iron utilization was as high as 0.8 mol of reduced Cr(VI) per mole of iron. It was also found that this composite material can be easily regenerated and reused for Cr(VI) reduction without significant loss of efficiency.

Gallic acid (GA), a natural plant polyphenol, was applied as amendment of Fe(III)/persulfate (PS) system for ibuprofen (IBP) degradation in this study. The impacts of all agentia (GA, Fe(III), PS) concentration and initial pH values on IBP removal efficiency were investigated, and their corresponding observed pseudo-first-order rate constants (kₒbₛ) were calculated. The addition of GA has significantly improved elimination efficiency of IBP due to the enhanced Fe(III)/Fe(II) cycle. Electron paramagnetic resonance (EPR) results confirmed that SO₄•⁻, HO• and O₂•⁻ were involved in GA/Fe(III)/PS system. However, quenching experiments further affirmed the impact of SO₄•⁻ and HO• towards IBP decomposition instead of O₂•⁻, with contribution ratio to IBP removal was 69.12% and 30.88%, respectively. SO₄•⁻ was the main radicals formed by directly activation of PS with Fe(II), while HO• was the transformation product of SO₄•⁻. Based on instrumental analysis (stopped-flow UV–vis spectrum and MS) and theoretical calculation, the potential reaction mechanism between GA and Fe(III) in the presence of PS was further proposed. GA complexed with Fe(III) firstly and the Fe(III)-GA complex was then converted into quinone substance, accompanied by the generation of Fe(II). Furthermore, the application of GA extended the optimal pH range to neutral as well, which made it a promising treatment in practical application.

This study was conducted to identify the bioactive phytochemicals in Salvia officinalis essential oil, to determine the polyphenols in the aqueous extract (SOE), and to evaluate their protective role against cadmium (Cd)-induced oxidative damage and genotoxicity in rats. Six groups of female rats were treated orally for 2 weeks including the control group, CdCl₂-treated group, SOE-treated groups at low or high dose (100 and 200 mg/kg b.w), and CdCl₂ plus SOE-treated groups at the two doses. The GC-MS analysis identified 39 compounds; the main compounds were 9-octadecenamide, eucalyptol, palmitic acid, and oleic acid. However, the HPLC analysis showed 12 polyphenolic compounds and the majority were coumaric acid, chlorogenic acid, coffeic acid, catechin, vanillin, gallic acid, ellagic acid, and rutin. In the biological study, rats received CdCl₂ displayed severe disturbances in liver and kidney indices alanine aminotransferase (ALT), aspartate aminotransferase (AST), albumin (Alb), total protein (TP), total bilirubin (T. Bil), direct bilirubin (D. Bil), creatinine, uric acid, and urea, lipid profile, tumor necrosis factor-alpha (TNF-α), alpha-fetoprotein (AFP) and CEA), glutathione (GSH), glutathione peroxidase (GPx), superoxide dismutase (SOD) and catalase (CAT), malondialdehyde (MDA), nitric oxide (NO), gene expressions, DNA fragmentation, and histological alterations in the liver and kidney tissue. SOE showed a potent antioxidant and mitigated these alterations in serum and tissue. Moreover, the high dose succeeded to normalize most of the tested parameters and histological features. It could be concluded that S. officinalis is a promising source for bioactive compounds with therapeutic benefits against environmental toxicants.

A novel bio-based polymeric adsorbent was fabricated and used for the removal of methylene blue (MB) from aqueous solutions. The method includes the synthesis of polymeric adsorbent from biocompatible chemicals such as poly(vinyl alcohol) (PVA) and 3,4,5-trihydroxybenzoic acid (gallic acid, GA) by using acid catalyzed esterification reaction. The obtained PVA/GA adsorbent was successfully characterized by the spectral, morphological, and thermal investigations using FTIR, SEM, DSC, and TGA. In the batch experiments, the adsorption performances of PVA/GA for MB were systematically investigated at various dye concentration, pH, contact time, and temperature conditions. The adsorption capacity of the PVA/GA reached a maximum value of 633.3 mg g⁻¹ at 25 °C. Possible reasons for high adsorption capacity of PVA/GA may be that the porosity and functional groups of PVA and GA afford sufficient active spots to advance the affinity of MB to the surface of adsorbent. The reusability efficiency of the adsorbent maintained above 96% after four adsorption–desorption cycles. In the data of adsorption process, it was most consistent with the Langmuir isotherm and pseudo-second-order kinetic models. Furthermore, it was confirmed that the adsorption is spontaneous and favorable from the thermodynamic point of view. The results demonstrated that the low-cost PVA/GA adsorbent system is simple to prepare and operate and exhibits promising properties as a reusable adsorbent for removal of hazardous dyes from aqueous solutions.

Diverse aromatic mediators have often been used to increase the degradation of organic pollutants by Fenton reaction (Fe²⁺ + H₂O₂ → Fe³⁺ + HO● + HO⁻). The presence of reducing mediators can minimize the accumulation of Fe³⁺ in solution, which leads to accelerated Fe²⁺ regeneration and enhances the generation of reactive oxygen species, such as the HO● radical, i.e., the strongest oxidant in Fenton-based processes. On the other hand, a few non-reducing compounds can be converted into reducing intermediates during reactions, in addition to assisting degradation processes. Therefore, the influence of aromatic mediators, reducers and non-reducers, on decolorization kinetics of Bismarck Brown Y (BBY) dye oxidized by Fenton processes (Fe²⁺/H₂O₂, Fe³⁺/H₂O₂) has been investigated herein by using data from a previous study that had been developed by the present research group. In general, the second-order reaction kinetic model was better fit to the experimental data. Improvements in apparent second-order rate constants (k₂) were observed due to the presence of mediators. Reducers were more effective than non-reducers in increasing k₂ values. In another kinetic model, BMG, maximum oxidation capacity was increased due to the presence of mediators. In a new set of experiments, a decrease in apparent activation energy was verified due to introducing mediators into reactions initially containing either Fe²⁺ or Fe³⁺ as catalysts to oxidize BBY at different temperatures. This indicates that the tested mediators, two reducers (hydroquinone, gallic acid) and a non-reducer (salicylic acid), can decrease the energy barrier to allow Fenton reaction to oxidize dyes more effectively.

Emphysema is associated with an abnormal airspace enlargement distal to the terminal bronchioles accompanied by destructive changes in the alveolar walls and chronic inflammation. Air pollution can cause respiratory diseases such as chronic obstructive pulmonary disease (COPD) and emphysema in urban areas. As a natural antioxidant compound, gallic acid may be effective in controlling inflammation and preventing disease progression. In this research, we investigated the protective role of gallic acid in the inflammatory process and the possible signaling pathway in the elastase-induced emphysema. Forty-eight rats were divided into six different groups including the following: control, gallic acid (7.5, 15, and 30 mg/kg), porcine pancreatic elastase (PPE), and PPE+gallic acid 30 mg/kg. Oxidative stress indexes such as malondialdehyde and antioxidant enzyme activity were measured in all groups. The gene expression levels of heme oxygenase-1 (HO-1), nuclear factor (erythroid-derived 2)-like 2 (Nrf2), and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) were determined as key regulators of antioxidant and inflammation system. The PPE group showed pulmonary edema and a significant change in arterial blood gas values, which was associated with decreased antioxidant activity of enzymes and changes in NF-κB, HO-1, and Nrf2 gene expression in comparison to the control group. Co-treatment with gallic acid preserved all these changes approximately to the normal levels. The results confirmed that elastase-induced emphysema leads to lung injuries, which are associated with oxidative stress and inflammation. Also, the results suggested that gallic acid as a natural antioxidant agent can modulate the Nrf2 signaling pathway to protect the lung against elastase-induced emphysema. Therefore, we documented the evidence for the importance of NF-κB inhibitors and Nrf2 activators as a target for new treatments in respiratory dysfunction caused by oxidative agents.

This study proposed the optimization of a laccase-mediator system to reduce pesticide levels (bentazone, carbofuran, diuron, clomazone, tebuconazole, and pyraclostrobin) on aqueous medium. Firstly, the mediator concentration of 1 mM was established (average removal of 36%). After that, seven redox-mediating compounds, namely, 2,20-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt, caffeic acid, chlorogenic acid, p-coumaric acid, ferulic acid, gallic acid, protocatechuic acid, and vanillin, were compared regarding their removal efficiency. The highest removal (77%) was achieved with the laccase-vanillin system. After this screening, the optimization was carried out by a 2² full factorial design. Variables under study were the enzyme (laccase) activity and vanillin concentration. Maximum removal (53–85%) was achieved with 0.95 U/mL laccase and 1.8 mM vanillin. Pesticide removal in reaction media was fitted to the first-order kinetics equation with an average half-time life of 2.2 h. This is the first study of the use of this natural compound as a mediator in the degradation of the pesticides under investigation. The results of this study contribute, with alternative methods, to decrease pesticide levels since they are highly persistent in aqueous samples and, as a result, mitigate the environmental impact.

The photocatalytic degradation effectiveness of six selected typical phytotoxic substances (ferulic, benzoic, gallic, salicylic, tannic, and acetic acid) by two levels of 10 nm TiO₂ (11 and 22 g/m²) immobilized on tiles under 254 nm of UV light irradiation was investigated. The results showed that the immobilized nano-TiO₂ significantly degraded all phytotoxic substances dissolved in distilled water, and the cumulative degradation rates of ferulic, benzoic, gallic, salicylic, tannic, and acetic acid reached 22.2, 33.6, 48.2, 56.9, 57.5, and 76.0 % after 6 h of treatment, respectively. Furthermore, the cumulative degradation rates of six phytotoxic substances by immobilized nano-TiO₂ were different remarkably, i.e., salicylic acid > benzoic acid, gallic acid > ferulic acid, acetic acid > tannic acid. The maximal photocatalytic degradation efficiencies of all phytotoxic substances appeared at the first 2 h in the three experiments. During the 6-h treatment period, the photocatalytic degradation efficiency of all phytotoxic substances decreased gradually. There was no significant difference in the photocatalytic degradation of benzoic acid and ferulic acid between the two levels of immobilized nano-TiO₂ treatments, whereas a significant difference was found in the photocatalytic degradation of salicylic acid, gallic acid, tannic acid, and acetic acid. In a word, nano-TiO₂ photocatalysis is an effective method to degrade phytotoxic substances. And the photocatalytic degradation effectiveness of six typical phytotoxic substances may be related to their structures.