Ultrapure Water Research Articles

Evaluation of the physicochemical properties of intracanal medications used in traumatized teeth

Aim: The aim of the present study was to evaluate the solubility, flow and radiopacity of Calen (SS White Artigos Dentários Ltd, Rio de Janeiro, Brazil), Calen with zinc oxide (Calen/ZnO), calcium hydroxide + zinc oxide + 2% chlorhexidine (CH/ZnO/CHX), Calplus and Ultracal XS. Methods: 28 bovine incisor specimens were standardized, instrumented and filled with pastes with the aid of a centrix syringe. To assess solubility, the root canals of acrylic teeth (N = 10) were filled with the previously mentioned pastes and scanned by using micro–computed tomography before (initial) and after 7 days of immersion in ultrapure water. The solubility of each specimen was the difference between the initial and final volume. Flow properties were analysed according to the ISO 6876/2012 standard. Radiopacity was radiographically analysed by using Image J software. Data were submitted to analysis of variance and Tukey’s test (alpha 5%). Results: CH/ZnO/CHX and Calplus presented similar values regarding radiopacity. The group composed of Calen paste showed higher flow values. As for solubility, CH/ZnO/ CHX showed lower volume loss, but there was no statistical difference compared to other medications. Conclusion: The medication composed of calcium hydroxide, zinc oxide and 2% chlorhexidine is a suitable alternative for use in traumatized teeth.

Investigation of short-term chemical changes in stable ruthenium added to soil by using X-ray absorption fine-structure analysis.

Radioactive ruthenium may be accidentally released from spent nuclear fuel reprocessing plants to the surrounding environment. However, research on the chemical behavior of radioactive Ru in the environment is limited, and the complex chemical properties of this element complicate the application of extraction methods for the analyses of its chemical forms. To obtain basic information regarding the outcome of radioactive Ru in the environment, we investigated the changes in the form of stable Ru added to soil through X-ray absorption fine-structure (XAFS) analysis. This study uses ruthenium tetroxide (RuO4), ruthenium dioxide (RuO2), ruthenium nitrosyl nitrate (Ru(NO)(NO3)3) and ruthenium chloride (RuCl3) as test sources. These are added to ultrapure water, soil solution or fresh soil samples, which are analyzed using XAFS immediately or 5 days after Ru addition. The Ru K-edge X-ray absorption near edge structure spectra acquired immediately after Ru addition differed with respect to the source. The XAFS results suggest that RuO4 immediately changes to tetravalent form after deposition from air to soil. For RuCl3, the ionic structure in the vicinity of Ru is affected by the soil even if the valence does not change immediately. By contrast, RuO2 and Ru(NO)(NO3)3 are highly stable in soil. The results show that the chemical forms of RuO2 and Ru(NO)(NO3)3 added to the soil solution and soil are retained for 5 days, whereas those of RuCl3 and RuO4 are affected by the soil solution and soil within a short period. These results emphasize the need to focus on the chemical form of Ru deposits and the form change after Ru addition when investigating the environmental fate of radioactive Ru.

Ultrasound-Assisted Community Bureau of Reference (BCR) Procedure for Heavy Metal Removal in Sewage Sludge

Sewage sludge (SS) resulting from wastewater treatment plants (WWTP) is commonly applied worldwide as a fertilizer in agriculture. This can be done following a rigorous analysis of the sewage sludge composition. Due to its toxic potential, heavy metal ion content is one of the key parameters to test when evaluating SS sample usage as fertilizer. The distribution of metals present in SS samples produced by five municipal WWTPs in Romania was studied. To obtain information regarding metal distribution in SS, a modified ultrasound-assisted extraction procedure of the Community Bureau of Reference (BCR) was employed for As, Cd, Cr, Cu, Mo, Ni, Pb, Zn, and Co quantitation. Concentrations of these metals were measured using ICP-EOS spectrometry. Method extraction accuracy was verified using CRM-483 certified reference material. Results show that extraction efficiency was lowest for the exchangeable fraction for all studied metals. The detected ion metals were found distributed in fractions (F) 2 and 3, which are unavailable for plants and groundwater under natural environmental conditions. One noteworthy finding was that using ultrapure water for the leachate test resulted in low metal solubility, indicating slight metal desorption in real environmental samples. Furthermore, maize stalk bio-adsorbent was used to minimize metal ion content in WWTP leachate samples produced by the storage of SS in terms of metal ion adsorption.

Degradation of enrofloxacin by Fe0 activated PDS.

In this paper, the effect of zero-valent iron (Fe0) activated persulfate (PDS) on the removal of enrofloxacin (ENR) was investigated, and the effect and mechanism were analyzed by exploring the effects of Fe0 concentration, PDS concentration, pH, and the influence of anion and aqueous matrix on the removal of ENR by the Fe0/PDS system. The results showed that when [ENR] = 20 µmol/L, [Fe0] = 0.15g/L, [PDS] = 0.4 mmol/L, the removal rate of ENR was 85.3% at 90min, the mainradicals were HO•, SO4•- and O2•-. At the same time, the system had a good mineralization effect (TOC removal rate > 40%), in addition, the system did not show obvious toxicity to soil microorganisms after the reaction, furthermore the Fe0/PDS system had a good removal effect on ENR in a wide pH range (4 ≤ pH ≤ 10). There is basically no difference in the removal rate of Fe0/PDS system in ultrapure water and river water.The results of this experiment could provide a reference for the removal of antibiotics based on advanced oxidation techniques based on SO4•-.

Degradation of extracellular antibiotic resistance genes using peracetic acid (PAA) and performic acid (PFA)

Antibiotic resistant bacteria (ARB) associated infections are identified as a major threat to human health in the 21st century. Wastewater contains antibiotic resistance determinants and they are discharged to aquatic environments with treated or untreated effluents. These antibiotic resistance determinants can be taken up by environmental bacteria via horizontal gene transfer (HGT) and they can become antibiotic resistant. Among antibiotic resistance determinants, extracellular DNA containing antibiotic resistance genes can be up taken by environmental bacteria via natural transformation. Therefore, we evaluated the suitability of low-cost disinfectants peracetic acid (PAA) and performic acid (PFA) on inactivating total and functional extracellular ARGs in ultrapure water and secondary wastewater effluent matrices using pUC19 as a model ARG. Performance of PAA and PFA in inactivating extracellular ARGs was compared with the performance of free chlorine disinfection. RT-qPCR results showed that inactivation of ampR gene in pUC19 plasmid suspended in ultrapure water and wastewater secondary effluent by free chlorine was higher compared to PAA and PFA. However, the reduction of functional pUC19 by PAA and PFA were comparable to free chlorine. Transformation frequency of pUC19 treated by PAA and PFA achieved the maximum possible reduction within a shorter time compared to free chlorine treatment, highlighting the possibility of having disinfection chambers with smaller footprints in wastewater treatment plants. These results suggest the suitability of PAA and PFA for inactivation of ARGs in aquatic samples as alternative disinfectants to free chlorine.

Fault Detection Technology for Ultrapure Water Plant using Virtual Sensors for Pressure Control Valve and Indicators in Return Line

Objectives:This study aims to propose a technology that utilizes virtual sensors to quickly and accurately diagnose faults in valves and measurement devices that may occur in the return line of an ultrapure water plant.Methods:The empirical equations were derived, and the error range was calculated using operational data collected from three pieces of equipment (pressure control valve, pressure transmitter, and flow transmitter) in the recovery system of the ultrapure water process. Based on this, a virtual sensor is established.Results and Discussion:It was confirmed that the utilization of 24-hour data collected from the operation of the ultrapure water plant was enough to establish virtual sensors and could also estimate monthly data with high accuracy. In Phase 1, the fault diagnosis technology was found to estimate values more accurately and had a meaningful margin of error compared to Phase 2.Conclusion:It was possible to develop a fault detection technology using the virtual sensor derived from the empirical equation. The technology showed high performance in detecting anomalies in the flow meter and pressure control valve opening but had limitations in estimating consistently pressure values. Additionally, considering that there was no issue in estimating monthly data using the equations derived using 24 hours operational data. The fault detection algorithm could be used continuously if the empirical equations are updated by collecting a day's data when operating conditions change.

Changes in the relaxivity of water-organic solvent miscible systems: Hidden forces beyond metal ions.

The relaxivity of magnetic resonance imaging (MRI) contrast agents is primarily attributed to metal ions such as gadolinium (Gd) and iron. However, the impact of organic solutes on relaxivity, particularly through alterations in water molecule dynamics, has not been thoroughly investigated. This research was aimed to explore how organic solutes affect the relaxivities of water and Gd-based contrast agents (GBCAs), potentially revealing new aspects for the development of contrast agents. To investigate the effects of different proportions of water-soluble organic solvents mixed with pure water and GBCA on T1 and T2 relaxivities. Ethanol, dimethyl sulfoxide (DMSO), 1,4-dioxane, glycerin, ethylene glycol, diethylene glycol, polyethylene glycol (PEG) 200, and PEG 400 were mixed with ultrapure water in various ratios (100:0, 90:10, 80:20, 70:30, 60:40, 50:50, 40:60, 30:70, 20:80, 10:90, 0:100). GBCA was added to these mixtures at a concentration of 0.05 mmol/L. The mixtures underwent T1 and T2 mapping scans using a 3.0 Tesla MRI machine, and the relaxivities R1 (1/T1) and R2 (1/T2) were calculated and compared. The relaxivity R1 of ethanol, 1,4-dioxane, and DMSO mixtures with water or GBCA, as well as R2 of DMSO mixtures with GBCA, initially increased and then decreased. Conversely, R1 and R2 increased significantly with higher proportions of diethylene glycol, PEG 200, and glycerin in the mixtures with GBCA. The increase in relaxivity R1 was correlated with greater viscosity. When the proportion of DMSO and diethylene glycol exceeded 20%, minimal variability in R2 was observed as the water content decreased. Adding organic solvents to water and paramagnetic relaxation reagents could alter T1 and T2 relaxivities, suggesting potential new directions for modifying current contrast agents. Additionally, increasing the viscosity of the contrast agent was found to enhance the relaxivity.

Elucidating silanol removal in MFI nanosized zeolites through controlled post-synthesis hydrothermal treatments

The rational control of silanol groups is still an elusive dream in zeolite synthesis. To enhance our understanding of this phenomenon, we have performed various hydrothermal post-synthesis treatments on nanosized Silicalite-1 using sodium molybdate, sodium chloride, and ultrapure water to evaluate the alteration of silanol content. All treated samples exhibited a phase transition from orthorhombic to monoclinic confirmed by X-ray diffraction (XRD). Fourier-Transform Infrared (FTIR) and solid-state Nuclear Magnetic Resonance (NMR) spectroscopy showed a decrease in the concentration of silanol groups in the post treated samples. The treatment with sodium molybdate leads to the removal of approximately 98% of the silanol groups, while the samples treated with sodium chloride and ultrapure water showed a decrease of 90% and 20% respectively, compared to the parent silicalite-1. Additionally, the results from pyridine adsorption followed by FTIR show that the Parent-Silicalite-1 and the H2O-Silicalite-1 samples contain a significant amount of defects, requiring 13.55 and 11.18 μmol, respectively, to saturate all the unsymmetrical bridging sites, while for the sample treated with sodium chloride only 1.07 µmol is needed to saturate all siloxane sites. In contrast, the treatment with sodium molybdate produced a free-defects zeolite. Molybdenum was found to contribute to the removal of both weak and strong hydrogen-bonded silanol groups through its insertion into the zeolite framework, while sodium played a significant role in condensing open bridges within the zeolite framework and removing less weak and strong hydrogen bonded silanol groups. This condensation of silanol groups seems to be facilitated by the polarization of silanol groups in presence of Na+ promoting the formation of siloxy groups that eventually condense easily with adjacent SiOH groups, liberating water molecules during the activation process of the samples.

In vitro spectroscopic analysis of the chemical interaction between calcium hypochlorite and chlorhexidine.

This study aimed to identify the chemical composition resulting from the chemical interaction between calcium hypochlorite [Ca(OCl)2] and chlorhexidine (CHX) using different 1H and 13C nuclear magnetic resonance spectrometry (NMR), correlated two-dimensional spectroscopy (2D COSY), heteronuclear single quantum coherence (HSQC), and Fourier Transform Infrared Spectroscopy (FTIR) experiments. The 5.25% Ca(OCl)2 was mixed with 2% CHX in a 1:1 ratio, obtaining an orange-brown precipitate that was filtered, washed in ultrapure water, dried and characterized by 1H and 13C NMR, 2D COSY, HSQC and FTIR. One-dimensional and two-dimensional NMR spectra demonstrated the chemical changes around the protons and carbon atoms of the initial CHX and after reacted with Ca(OCl)2. These techniques and FTIR show that the interaction generated two by-products from the degradation of CHX, none of which were parachloroaniline (PCA) despite both products obtained being substituted benzene compounds. Using NMR and FTIR data together with a previously proposed catalytic cleavage degradation mechanism for CHX, the products appear to be parachlorophenylurea (PCU) and parachlorophenylguanidyl-1,6-diguanidyl-hexane (PCGH). Therefore, this in vitro study demonstrated that the precipitate formed from the chemical interaction between Ca(OCl)₂ and CHX results in two by-products, PCU and PCGH, neither of which is PCA. Due to the absence of cytotoxicity studies on the products generated from the combination of Ca(OCl)₂ and CHX, an intermediate rinse with an inert solution is recommended to remove these compounds from the root canals.

Degradation of ciprofloxacin by hydrogen peroxide activated with pyrite under simulated sunlight

Ciprofloxacin (CIP) residues in the environment pose risks to both human health and ecosystems. In this study, we explored the effect of hydrogen peroxide (H2O2) on CIP degradation, activated by pyrite (FeS2) under simulated sunlight. XRD, XRF, EDS, XSP, DRS, and PL tests confirmed the high purity of FeS2 and its photocatalytic properties. With [CIP] = 30 μM, [FeS2] = 0.2 g/L, [H2O2] = 0.2 mM, CIP removal reached 87.6 %. The removal rate of TOC reached 55.3 % after 60 min of light exposure, and hydroxyl radicals (OH) contributed 72.7 % to the process. H2O2 utilization was 67.5 %, and the system operated effectively across a pH range of 2.00 to 8.00. CIP removal in river water reached 87.9 % after 3 h of light exposure, though the degradation was slower than in ultrapure water. Cl−, SO42−, and NO3− had little effect on degradation, whereas H2PO4−, CO32−, and HCO3− significantly inhibited the process as their concentrations increased. In livestock wastewater, the simulated sunlight-FeS2/H2O2 system was less effective, but after diluting the wastewater 100 times, CIP removal reached 87.6 % after 60 min. The degraded solutions showed no significant toxicity. These findings suggest that FeS2, combined with simulated sunlight, can effectively catalyze low concentrations of H2O2 to produce OH radicals, removing antibiotics from livestock wastewater.

Construction of all-solid-state ion-selective sensors using electrolyte-containing polymers.

All-solid-state NO3-, K+, NH4+, Na+, and Ca2+ ion-selective sensors (ISEs) were prepared using polyvinyl butyral (S-LEC®K KX-5). In the present case, polyvinyl butyral was used as a porous material to keep the internal solution of the respective ISE. All sensors exhibited near-Nernst responses in the concentration region between approximately 10-5 and 0.1moldm-3. To avoid the influence of KCl as interfering ions, MgSO4 was used as an electrolyte within the salt bridge. Although the liquid junction potential was generated, the potential difference was stabilized within about few minutes. The NO3--ISE showed high stability with no potential drift during 12h of continuous measurements and maintained high sensitivity even after 3weeks of storage in ultrapure water. Solidification of the internal solution is expected to make the sensor smaller and increase its mechanical strength. As an actual measurement, the sodium concentration in plasma samples using the Na+-ISE was measured to confirm agreement with literature values.

Assessment of Heavy Metal Contamination in Combretum micranthum Leaves and Decoctions: Implications for Human Health

Combretum micranthum is a well-known medicinal plant in Africa and the decoction of its leaves is used as a drink or to treat various diseases such as malaria, high blood pressure and liver disorders, among others. Due to its high consumption by all sections of the Senegalese population, we felt that its heavy metal intake should be examined to see its impact on health. Leaves of two species of Combretum micranthum produced in the central (I) and southern (II) regions of Senegal and their decoctions in ultrapure water (Ii) and (IIi) were analyzed for 12 elements (Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Ag, Cd, Pb, Bi) by inductively coupled plasma optical emission spectrometer (ICP-OES). The concentrations of heavy metals (μg/g) are in the ranges 2.55 – 84.19 for Cr, 5.21 – 379.72 for Mn, 0.00 – 317.80 for Fe, 0.08 – 1.08 for Co, 1.54 – 8.88 for Ni, 1.75 – 8.08 for Cu, 0.91 – 9.70 for Zn, 0.00 – 0.16 for Cd, 0.46 – 0.84 for Pb. As, Ag and Bi are below detectable limits in any of the samples by ICP-OES analysis. Among all samples, manganese content was highest and represented 46.85% for I , 64.18% for II , 86.88% for Ii and 46.27% for IIi , of the total heavy metal concentrations. The results showed that the leaves of both varieties of Combretum micranthum and decoctions made from these leaves contain heavy metal levels lower than the values recommended by the WHO for consumed medicinal plants. Overall, Variety I harvested from peri-urban areas contains more metals than Variety II harvested from forest.

Effect of the Dispersion Medium on NMR Relaxation Properties of Superparamagnetic Iron Oxide Nanoparticles between 0.24 mT and 14.1 T.

Due to weak exchange interactions, magnetite particles at a critical diameter of about 20 nm are considered monodomain. At this size, they exhibit a phenomenological magnetic property called superparamagnetism, making them useful as magnetic resonance imaging contrast agents, or MRI CAs. However, questions persist regarding the impact of using different physiological solvents and varying the environment in which these particles are dispersed on their performance, determined by their relaxivity. A colloidal suspension of superparamagnetic iron oxide nanoparticles (SPIONs) electrostatically stabilized by citrate ligand was synthesized using a fast, reliable, and reproducible developed microwave approach, ensuring high stability over time at pH 7. We studied the effects of three physiological media on these MRI CAs. Ultrapure water was used for the synthesis, while phosphate-buffered saline and physiological liquid were used to disperse the nanoparticles, as these media contain essential electrolytes for the functioning of the human body. The SPIONs underwent systematic characterizations to determine their physicochemical and magnetic properties. This study reports the longitudinal relaxivities of SPIONs at medically relevant magnetic field strengths. Field dependence of their relaxivity (efficacy) was evaluated using a nuclear magnetic resonance dispersion (NMRD) profile measured over a wide range of proton resonance frequencies between 5 kHz and 600 MHz. The Roch et al. model (Roch, A.; et al. J. Chem. Phys., 1999, 110, 5403-5411) was used to analyze the NMRD profile and evaluate the impact of SPIONs on water proton relaxation in the different redispersion media. It was observed in this study that the dynamics of water protons are not influenced by the redispersion media of these citrate-coated SPIONs. However, the presence of salt ions notably reduces their relaxivities by lowering the saturation magnetization of SPIONs.

Development, Validation, and Greenness Assessment of Eco-Friendly Analytical Methods for the Determination of Abiraterone Acetate in Pure Form and Pharmaceutical Formulations

This study presents the development and validation of environmentally friendly analytical methods for quantifying Abiraterone Acetate (AA) in both its pure form and commercial pharmaceutical formulations. An optimized High-Performance Liquid Chromatography (HPLC) method was developed using an Agilent Extend C18 column (250 mm × 4.6 mm, 5 μm) at 25 °C. The mobile phase consisted of formic acid and ethanol in isocratic mode, with a flow rate of 1.0 mL min−1, and detection was performed at 253 nm. The spectrophotometric method involved a comprehensive evaluation of AA’s spectral properties in various solvents, with ultrapure water providing the most suitable spectra for analysis at 253 nm. Both methods were validated according to ICH guidelines, demonstrating selectivity, linearity, accuracy, precision, detection and quantification limits, and robustness, with correlation coefficients exceeding 0.999 across the 5–30 μg mL−1 concentration range. Comparative statistical analysis using Student’s t-test and Fisher’s F-test showed no significant differences between the two methods. The environmental impact of both methods was assessed using AGREE and GAPI software, confirming their sustainability. These validated methods offer reliable and eco-friendly approaches for the quantitative analysis of AA in tablet formulations, promoting safer and greener laboratory practices in pharmaceutical analysis.

Ameliorative effects of Penthorum chinense Pursh on insulin resistance and oxidative stress in diabetic obesity db/db mice.

Penthorum chinense Pursh (PCP), a medicinal and edible plant, has been reported to protect against liver damage by suppressing oxidative stress. Type 2 diabetes mellitus (T2DM) is associated with liver dysfunction and oxidative stress. In the present study, we aim to investigate the hypoglycemic effect of PCP on db/db mice and further explore the underlying mechanisms. Thirty-two db/db mice were randomized into four groups, including a diabetic model control group (MC) and three diabetic groups treated with low (LPCP, 300 mg/kg/d), medium (MPLP, 600 mg/kg/d), and high doses of PCP (HPCP, 1200 mg/kg/d), and the normal control group (NC) of eight db/m mice were included. Mice in the NC and MC groups received the ultrapure water. After four weeks of intervention, parameters of fasting blood glucose (FBG), insulin resistance (IR), blood lipid levels, hepatic oxidative stress, and enzymes related to hepatic glucose metabolism were compared in the groups. PCP administration significantly reduced FBG and IR in diabetic db/db mice, and improved hepatic glucose metabolism by increasing glucose transporter 2 (GLUT2) and glucokinase (GCK) protein expression. Meanwhile, PCP supplementation ameliorated hepatic oxidative stress by decreasing malonaldehyde content and increasing the activities of superoxide dismutase and glutathione peroxidase in db/db mice. Furthermore, PCP treatment reduced obesity and food intake in db/db mice, and improved dyslipidemia demonstrated by increasing high-density lipoprotein cholesterol (HDL-C) while decreasing total cholesterol (TC), triglyceride (TG), and low-density lipoprotein cholesterol (HDL-C). All doses of PCP treatment decreased the values of LDL-C/HDL-C in a dose-response relationship. PCP significantly alleviated hyperglycemia, hyperinsulinemia, hyperlipidemia, and obesity, inhibited hepatic oxidative stress, and enhanced hepatic glucose transport in T2DM mice. Based on the above findings, the hypoglycemic effect of PCP may be attributed to the activation of the GLUT2/GCK expression in the liver and the reduction of hepatic oxidative stress.

Biostability assessment of ultrapure water piping materials in the semiconductor industry and their susceptibility to Ralstonia growth

The pipes used for ultrapure water (UPW) distribution are constructed using high-quality materials to ensure purity. However, there remains a risk of contamination based on the pipe type. This study is the first to comprehensively evaluate the biological implications of various UPW pipe materials used in the semiconductor industry. The results showed that Polyvinylidene fluoride (PVDF) exhibited lower organic carbon leaching (0.08 mg/L) and a reduced biomass formation potential (BFP) (approximately 5 × 105 cells/cm2) compared to chlorinated polyvinyl chloride (CPVC) pipes. In particular, Ralstonia, an oligotrophic bacterium commonly found in UPW systems, formed a significant biofilm on pipe surfaces, notably in stainless steel (SUS) and CPVC pipes. Furthermore, particle contamination, a critical concern in semiconductor manufacturing, was investigated, focusing on potential contamination sources generated by pipe leaching and the presence of bacteria. The bacterial composition of the selected UPW was investigated, revealing Herbaspirillum, a nitrogen-fixing bacterium, as the dominant species, account for 66.15 %. Notably, the composition of the feedwater was different from that of the UPW. This study also highlights the limitations of culture-based methods, particularly in detecting bacteria under oligotrophic conditions, which are often unculturable. Flow cytometry (FCM) shows promise for the quick detection of bacterial contamination by providing total cell counts. Moreover, cytometric fingerprinting analysis revealed phenotypic differences between the communities. Nevertheless, further development of a simplified and widely applicable cell counting protocol is required for its effective integration into UPW production.

Potential of solar photodegradation of antibiotics in shallow ditches: Kinetics, the role of dissolved organic matter and prediction models

Shallow ditches, which generally receive livestock or domestic sewage, are widely distributed in rural and suburban areas, making them important sites for antibiotic exposure. Because of the easy penetration of solar irradiation, the photochemical reactions of antibiotics tend to be active in shallow ditches. This study investigated the photodegradation potential of 21 commonly used antibiotics belonging to five categories in a typical shallow ditch by conducting simulated solar irradiation experiments. The influence of dissolved organic matter (DOM) in ditch water on the photodegradation of antibiotics was analyzed, and a model based on DOM changes was established to predict the degradation behavior of antibiotics. The results indicated that the degradation rates of different varieties of antibiotics in ultrapure water and ditch water followed the trend of fluoroquinolones > tetracyclines > sulfonamides > macrolides > lincosamides. In ditch water, direct photodegradation and photooxidation mediated by 3DOM∗ played predominant roles in the antibiotic photodegradation, whereas the contributions of singlet oxygen (1O2) and hydroxyl radicals (·OH) varied significantly depending on the reactivity of the antibiotics. A simple and effective model was proposed for predicting the photodegradation process of antibiotics in ditch water based on the degree of DOM photobleaching determined by excitation-emission matrix fluorescence spectroscopy coupled with parallel factor analysis. The prediction model was simplified by considering the similarity in photochemical properties within the same category of antibiotics and was validated by field tests. This study fills a critical research gap by evaluating the photodegradation of antibiotics in shallow ditches, thereby providing valuable insights into their fate and transport in shallow ditch water.

Wettability-dependent dissolution dynamics of oxygen bubbles on Ti64 substrates

In this study, the dissolution of a single oxygen bubble on a solid surface, here Titanium alloy Ti64, in ultrapure water with different oxygen undersaturation levels is investigated. For that purpose, a combination of shadowgraph technique and planar laser-induced fluorescence is used to measure simultaneously the changes in bubble geometry and in the dissolved oxygen concentration around the bubble. Two different wettabilities of the Ti64 surface are adjusted by using plasma-enhanced chemical vapor deposition. The dissolution process on the solid surface involves two distinct phases, namely bouncing of the oxygen bubble at the Ti64 surface and the subsequent dissolution of the bubble, primarily by diffusion. By investigating the features of oxygen bubbles bouncing, it was found that the boundary layer of dissolved oxygen surrounding the bubble surface is redistributed by the vortices emerging during bouncing. This establishes the initial conditions for the subsequent second dissolution phase of the oxygen bubbles on the Ti64 surfaces. In this phase, the mass transfer of O2 proceeds non-homogeneously across the bubble surface, leading to an oxygen accumulation close to the Ti64 surface. We further show that the main factor influencing the differences in the dynamics of O2 bubble dissolution is the variation in the surface area of the bubbles available for mass transfer, which is determined by the substrate wettability. As a result, dissolution proceeds faster at the hydrophilic Ti64 surface due to the smaller contact angle, which provokes a larger surface area.

Effects of water matrices on the removal of oxytetracycline antibiotic and total organic carbon (TOC) using four different oxidation processes

Antibiotic compounds are actively discharged into aquatic environments through wastewater, potentially contributing to the emergence of drug-resistant bacteria and associated health issues. Oxidation processes (OPs), including advanced oxidation processes (AOPs), have gained attention as promising methods for removing antibiotics from wastewater. In this study, we comprehensively compared the efficiencies of removing oxytetracycline (OTC) and total organic carbon (TOC) by four OPs. These processes include three AOPs: the ozone/hydrogen peroxide process (O3/H2O2), photo-Fenton reaction (Fe/H2O2/UV), and Fenton reaction (Fe/H2O2), and ozonation (O3) as a conventional OP. To evaluate the effects of different water matrices, the degradation experiments were conducted using ultrapure water and actual wastewater. All four OPs achieved over 99% OTC degradation within 15 minutes of the experiment. The photo-Fenton reaction exhibited the highest TOC removal rates (66% for ultrapure water and 74% for actual wastewater) after 210 minutes. Conversely, ozonation resulted in the lowest TOC removal rates (7% for ultrapure water and 10% for actual wastewater). Therefore, this study suggests that the photo-Fenton reaction may be most suitable for degrading OTC and removing TOC from wastewater.

Preparation and characterization of a novel green cinnamon essential oil nanoemulsion for the enhancement of safety and shelf-life of strawberries

This study aimed to optimize a novel green CEO nanoemulsions (CEO NEs) and explore its physicochemical properties and the effect on the shelf-life of strawberries during storage at environmental temperature (20–25 °C). We used CEO as oil phase and tea saponin (TS) as a natural surfactant to formulate the novel green CEO NEs, and its potential as an antimicrobial agent was also investigated. The results showed that CEO NEs had a droplet size about 170 nm with uniform distribution and regularly spherical. These CEO NEs exhibited excellent storage stability, thermal stability, pH stability and centrifugal stability. The antimicrobial test indicated that the minimal inhibitory concentration and the minimal bactericidal (fungicidal) concentration of CEO NEs against Escherichia coli, Botrytis cinerea and Aspergillus flavus were 17.81 μg/mL and 35.62 μg/mL, 35.62 μg/mL and 71.25 μg/mL, 2.23 μg/mL and 4.45 μg/mL, respectively, which were significantly lower than those of pure CEO (333.75 μg/mL and 667.5 μg/mL, 667.5 μg/mL and 1335 μg/mL, 41.72 μg/mL and 83.44 μg/mL). More interestingly, after soaking strawberries in CEO NEs for 2 min, the shelf-life of strawberries can be extended to 7 days at environmental temperature, and a lower rate of weight loss and mildew were showed in the group of CEO NEs than other control groups, especially the strawberries in ultrapure water group went bad first, obviously shranked, and contaminated by molds after 3 days. The above results indicate that CEO NEs prepared in this study has great potential as a new green antimicrobial agent in fruit preservation.