Water Solution Research Articles

Nitrite manipulation in water by structure change of plasma electrolysis reactor.

In this study, experimental reactors for cathodic nitrogen plasma electrolysis were designed by the composition of galvanic (voltaic) and electrolytic cells with wide and narrow connectors filled with tap water and agar solutions. The designed reactor can be used to simultaneously perform and manage nitrification in acidic and alkaline environments. According to the reactor's performance, it can be installed on the irrigation system and used depending on the soil pH of the fields for delivering water and nitrogen species that are effective in growth. The nitrification process was investigated by choosing the optimal reactor with a wide connector based on different changes in oxidation-reduction potential and pH on the anode and cathode sides. The nitrite concentration changed directly with ammonium and nitrate concentrations on the cathode side. It changed inversely and directly with ammonium and nitrate concentrations on the anode side respectively. Nitrite concentration decreased from 5.387 ppm with water connector, to 0.326 ppm with 20% agar solution, and 0.314 ppm with 30% agar solution connectors on the anode side. It increased from 0 ppm to 0.191 ppm with a water connector, 0.405 ppm with 20% agar solution, and 7.454 ppm with 30% agar solution connectors on the cathode side.

Combination of the degrading bacterium Bacillus cereus MZ-1 and corn straw biochar enhanced the removal of imazethapyr from water solutions

Long residual herbicide imazethapyr has caused a serious threat to subsequent sensitive crop plants and ecological security. Efficient immobilized microorganism technology offers a sustainable solution for remediating pesticides contamination. In this study, three corn straw biochars produced at 300℃, 500℃, and 700℃ were used as carriers to immobilize the imazethapyr degrading strain Bacillus cereus MZ-1, aiming to efficiently remove imazethapyr from the water environment. Response surface methodology was employed to optimize the best immobilization conditions based on the efficiency of imazethapyr removal. The results indicate that the biochar produced at 500 ℃ was the most effective carrier for immobilization, despite having a lower imazethapyr removal capacity compared to the biochar produced at 700 ℃. Additionally, the optimal strain addition amount was a suspension of strain MZ-1 (OD600=1) in a 3.5-fold biochar solution, and the best immobilized time was 18 h. The prepared immobilized MZ-1 achieved a maximum imazethapyr removal efficiency of 79.85 %. Moreover, the immobilized MZ-1 demonstrated enhanced detoxification efficacy against imazethapyr-induced harm in sensitive oilseed rape crops, surpassing the effects of using MZ-1 or biochar alone. Results of this work suggests biochar immobilized degradation strain MZ-1 is a highly effective in-situ remediation strategy for bioremediation of imazethapyr contamination.

Preparation and structural characteristics of polysaccharides from loquat peel waste, and their preliminary bioactivities.

Loquat peel, often as food waste, is a valuable source of bioactive polysaccharides. However, study of such polysaccharides is insufficient, leaving a significant gap in understanding their preparation, structure and bioactivities. In this study, three types of loquat peel polysaccharides (LPWP, LPHP and LPNP) were sequentially extracted using hot water, HCl and NaOH solutions, respectively. Among them, LPWP was the purest, with a yield of 3.4% and molecular weight of 470.6 kDa, and it differed from LPHP and LPNP in structure, as evidenced by Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy, which demonstrated that LPWP consisted of more arabinose (Ara) but less galacturonic acid, rhamnose and galactose, with molar percentages of 71.3%, 23.3%, 3.5% and 1.9%, respectively. Besides, LPWP also exhibited superior antioxidant and antihyperglycemic activities in vitro, particularly in inhibiting α-amylase and α-glucosidase. Methylation and nuclear magnetic resonance analysis confirmed that LPWP was a methyl-esterified pectic polysaccharide rich in branched arabinan, as evidenced by the notable proportion of α-Ara residues, including T-α-Araf, 1,5-α-Araf and 1,2,3,5-α-Araf, with molar percentages of 27.1%, 23.1% and 10.2%, respectively. AFM imaging further revealed its branched-chain morphology and aggregation behavior. This study highlights the potential of loquat peel polysaccharides as a bioactive ingredient with significant antioxidant and antihyperglycemic properties, particularly LPWP, which was found as a methyl-esterified pectic polysaccharide with abundant-branched arabinan. Our work provides valuable insights into the application of loquat peel polysaccharides in functional foods. © 2024 Society of Chemical Industry.

Toward Sustainable Water Solutions: A Review of Nanomaterials for Solar-Driven Water Harvesting

Toward Sustainable Water Solutions: A Review of Nanomaterials for Solar-Driven Water Harvesting

Oxidative stress-modifying effects of TiO2 nanoparticles with varying content of Ti3+(Ti2+) ions

Nanoparticles (NPs) with reactive oxygen species (ROS)-regulating ability have recently attracted great attention as promising agents for nanomedicine. In the present study, we have analyzed the effects of TiO2defect structure related to the presence of stoichiometric (Ti4+) and non-stoichiometric (Ti3+and Ti2+) titanium ions in the crystal lattice and TiO2NPs aggregation ability on H2O2- and tert-butyl hydroperoxide (tBOOH)-induced ROS production in L929 cells. Synthesized TiO2-A, TiO2-B, and TiO2-C NPs with varying Ti3+(Ti2+) content were characterized by x-ray powder diffraction, transmission electron microscopy, small-angle x-ray scattering, x-ray photoelectron spectroscopy, and optical spectroscopy methods. Given the role of ROS-mediated toxicity for metal oxide NPs, L929 cell viability and changes in the intracellular ROS levels in H2O2- and tBOOH-treated L929 cells incubated with TiO2NPs have been evaluated. Our research shows that both the amount of non-stoichiometric Ti3+and Ti2+ions in the crystal lattice of TiO2NPs and NPs aggregative behavior affect their catalytic activity, in particular, H2O2decomposition and, consequently, the efficiency of aggravating H2O2- and tBOOH-induced oxidative damage to L929 cells. TiO2-A NPs reveal the strongest H2O2decomposition activity aligning with their less pronounced additional effects on H2O2-treated L929 cells due to the highest amount of Ti3+(Ti2+) ions. TiO2-C NPs with smaller amounts of Ti3+ions and a tendency to aggregate in water solutions show lower antioxidant activity and, consequently, some elevation of the level of ROS in H2O2/tBOOH-treated L929 cells. Our findings suggest that synthesized TiO2NPs capable of enhancing ROS generation at concentrations non-toxic for normal cells, which should be further investigated to assess their possible application in nanomedicine as ROS-regulating pharmaceutical agents.

Promoting the circularity of ceramic materials through cold sintering of aggregates from construction and demolition waste

A ceramic composition containing 95 wt% of construction and demolition waste-like material was consolidated by cold sintering process at 200ºC using KOH water solutions as the liquid medium. The relative density of the samples reaches ∼ 90% of the theoretical one for process conditions of 600 MPa and 60 min. A post-annealing process at 1100ºC of the as-cold sintered samples causes a slight increase in the relative density and of their mechanical strength compared with conventionally sintered samples at 1100ºC and increases the shape factor of the Weibull distribution, thus increasing the reliability of the component. It is shown that cold sintering of the material avoids its high pyroplasticity, providing low shrinkage and reducing internal defects in the ceramic. This work represents the first exploration of the viability of manufacturing ceramic tiles with high recycled content contributing to the transition to a greener world.

Silicon Phthalocyanines Functionalized with Axial Substituents Targeting PSMA: Synthesis and Preliminary Assessment of Their Potential for PhotoDynamic Therapy of Prostate Cancer.

Photodynamic therapy (PDT) is a clinical modality based on the irradiation of different diseases, mostly tumours, with light following the selective uptake of a photosensitiser by the pathological tissue. In this study, two new silicon(IV)phtalocyanines (SiPcs) functionalized at both axial positions with a PSMA inhibitor are reported as candidate photosensitizers for PDT of prostate cancer, namely compounds SiPc-PQ(PSMAi)2 and SiPc-OSi(PSMAi)2. These compounds share the same PSMA-binding motif, but differ in the linker that connects the inhibitor moiety to the Si(IV) atom: an alkoxy (Si-O-C) bond for SiPc-PQ(PSMAi)2, and a silyloxy (Si-O-Si) bond for SiPc-OSi(PSMAi)2. Both compounds were synthesized by a facile synthetic route and fully characterized by 2D NMR, mass spectrometry and absorption/fluorescence spectrophotometry. The PDT agents showed a suitable solubility in water, where they essentially exist in monomeric form. SiPc-PQ(PSMAi)2 showed a higher singlet oxygen quantum yield ΦΔ, higher fluorescence quantum yields ΦF and better photostability than SiPc-OSi(PSMAi)2. Both compounds were efficiently taken up by PSMA(+) PC3-PIP cells, but not by PSMA(-) PC3-FLU cells. However, SiPc-PQ(PSMAi)2 showed a more specific photoinduced cytotoxicity in vitro, which is likely attributable to a better stability of its water solutions.

Comparison of DeNOx additives in SNCR fluidized bed boiler system

Due to decreasing BAT emission limits of NOx the owners of heating plant are looking for DeNOx solution, especially by solid fuel firing boilers. Fluidized-bed boil-ers combustion temperature is generally lower, and some primary precautions were sufficient. Nowadays lots of plants install secondary precautions (especially SNCR) into their boilers due to increasing periods of exceeding emission NOx limits. The article is about comparison of water solution of urea (41 % wt.), ammonium sulfate (33 % wt.) and am-monia (22 % wt.) and their utilization in SNCR technol-ogy. Laboratory determination specified exact content of functional substance and content of redox nitrogen. Also, significant content of heavy metals was not detected. Operational tests were realized in CFB coal-biomass boiler (steam parameters: 140 t·h-1, 525 °C, 12.5 MPa). Dosing of DeNOx additives were only during boiler per-formance higher than 92 %, for lower performance pri-mary precautions were sufficient. There was higher tem-perature through the combustion chamber during active SNCR dosing (877 °C, standard temperature 850 °C), alt-hough the amount of combustion air was increased. Com-plication connected with high emission of NH3 was not detected. Lower emission of CO was also detected. All three additives are suitable for application in SNCR technology. To reach emission limits were needed 3.7 l·h-1 of ammonia solution, 5.04 l·h-1 of urea solution and 5.74 l·h-1 of ammonium sulfate solution. After recal-culation it means 0.65 kg·h-1 (ammonia), 1.1 kg·h-1 (urea) and 0,38 kg·h-1 (ammonium sulfate) of redox nitrogen content.

Enhanced Photocatalytic Paracetamol Degradation by NiCu-Modified TiO2 Nanotubes: Mechanistic Insights and Performance Evaluation

Anodic TiO2 nanotube arrays decorated with Ni, Cu, and NiCu alloy thin films were investigated for the first time for the photocatalytic degradation of paracetamol in water solution under UV irradiation. Metallic co-catalysts were deposited on TiO2 nanotubes using magnetron sputtering. The influence of the metal layer composition and thickness on the photocatalytic activity was systematically studied. Photocatalytic experiments showed that only Cu-rich co-catalysts provide enhanced paracetamol degradation rates, whereas Ni-modified photocatalysts exhibit no improvement compared with unmodified TiO2. The best-performing material was obtained by sputtering a 20 nm thick film of 1:1 atomic ratio NiCu alloy: this material exhibits a reaction rate more than doubled compared with pristine TiO2, enabling the complete degradation of 10 mg L−1 of paracetamol in 8 h. The superior performance of NiCu-modified systems over pure Cu-based ones is ascribed to a Ni and Cu synergistic effect. Kinetic tests using selective holes and radical scavengers unveiled, unlike prior findings in the literature, that paracetamol undergoes direct oxidation at the photocatalyst surface via valence band holes. Finally, Chemical Oxygen Demand (COD) tests and High-Resolution Mass Spectrometry (HR-MS) analysis were conducted to assess the degree of mineralization and identify intermediates. In contrast with the existing literature, we demonstrated that the mechanistic pathway involves direct oxidation by valence band holes.

In Vitro Cytotoxicity and Pharmacokinetic Study for Bosutinib Solid Lipid Nanoparticles.

Bosutinib (BST) is a Biopharmaceutics Classification System Class II drug having very low solubility and high permeability. Low aqueous solubility and poor dissolution of BST lead to poor bioavailability, Thus, limited aqueous solubility is the bottleneck for the therapeutic outcome of BST. Animal data suggest that the absolute bioavailability of BST is about 14-34% due to an extensive first-pass effect. To overcome hepatic first-pass metabolism and to enhance oral bioavailability, lipid-based drug delivery systems such as solid lipid nanoparticles (SLNs) can be used. SLNs are submicron colloidal carriers having a size range of 50-1000 nm. These are prepared with physiological lipid and dispersed in water or aqueous surfactant solution. BST can be conveniently loaded into SLNs to improve the oral bioavailability by exploiting the intestinal lymphatic transport. An optimal system was evaluated for bioavailability study in rats compared with that of BST suspension (SUS). An in vitro cytotoxicity study was done by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay method through ATCC cell lines; the percent inhibition was more in SLN when compared with SUS. The pharmacokinetics of BST-SLNs after oral administration in male Wistar rats was studied. The bioavailability of BST was increased by 2.28 fold when compared with that of a BST SUS. The results are indicative of SLNs as suitable lipid-based carrier system for improving the oral bioavailability of BST.

The Important Role of Aquaglyceroporin 7 in Health and Disease

Aquaporins (AQPs) are highly conserved small transmembrane proteins that facilitate the transport of water and small solutes across cell membranes. Aquaglyceroporin 7 (AQP7), a significant member of the AQP family, is widely distributed throughout the body. For years, AQP7 was predominantly recognized for its role as a small-molecule transporter, facilitating the passage of small molecular substances. However, growing studies have revealed that AQP7 is also involved in the regulation of lipid synthesis, gluconeogenesis, and energy homeostasis, and it is intimately linked to a variety of diseases, such as obesity, type 2 diabetes mellitus, cardiovascular diseases, cancer, and inflammatory bowel disease. This article presents a comprehensive overview of the structure of AQP7, its regulatory mechanisms, its vital roles in both healthy and diseased states, and potential therapeutic advancements. We hope that these studies will serve as a valuable reference for the development of future treatments and diagnostic protocols targeting AQP7.

Investigation of kinetic mechanisms of photocatalytic hydrogen generation from formic aside using metal-ceramic composites under visible-light irradiation

Processes of photocatalytic hydrogen generation from the formic acid water solution under vis-light irradiation with tantalum contained metal-ceramic silicon nitride-based composites were investigated depending on pH of the solution and hydrogen peroxide adding. These compounds were obtained by self-propagated high temperature (SHS) synthesis in the way of the ferrosilicoaluminum (FSA) and silicon-aluminum powders ignition in a nitrogen atmosphere with the tantalum addition. During the investigation it was found out that the reaction rate of the hydrogen production without hydrogen peroxide can be described within the Langmuir–Hinshelwood mechanism. There is the reaction mechanism changing simultaneously with a formic acid concentration increasing in the presence of H2O2. The most significant reaction rate of hydrogen production from HCOOH is observed with the Fe-contained composite synthesized from FSA in the solution system without H2O2 addition, the reaction turns of frequency (TOF) is 4.55 µmol/min.

Gamma rays impact on 2D-MoS2 in water solution.

Two-dimensional transition metal dichalcogenides, particularly MoS2, are interesting materials for many applications in aerospace research, radiation therapy and bioscience more in general. Since in many of these applications MoS2-based nanomaterials can be placed in an aqueous environment while exposed to ionizing radiation, both experimental and theoretical studies of their behaviour under these conditions is particularly interesting. Here, we study the effects of tiny imparted doses of 511keV photons to MoS2 nanoflakes in water solution. To the best of our knowledge, this is the first study in which ionizing radiation on 2D-MoS2 occurs in water. Interestingly, we find that, in addition to the direct interaction between high-energy photons and nanoflakes, reactive chemical species, generated by γ-photons induced radiolysis of water, come into play a relevant role. A radiation transport Monte Carlo simulation allowed determining the elements driving the morphological and spectroscopical changes of 2D-MoS2, experimentally monitored by SEM microscopy, DLS, Raman and UV-vis spectroscopy, AFM, and X-ray photoelectron techniques. Our study demonstrates that radiolysis products affect the Molybdenum oxidation state, which is massively changed from the stable + 4 and + 6 states into the rarer and more unstable + 5. These findings will be relevant for radiation-based therapies and diagnostics in patients that are assuming drugs or contrast agents containing 2D-MoS2 and for aerospace biomedical applications of 2DMs investigating their actions into living organisms on space station or satellites.

Graphene oxide-containing chitosan@HKUST-1 beads with increased chemical stability for CO2 capture

HKUST-1 MOF was crystallized within chitosan matrix to form xerogel beads using an in-situ growth approach. Under mild conditions, CS@HKUST-1 xerogel beads exhibit high specific surface areas (SBET) up to 923 m2 g−1. By further incorporating graphene oxide (GO) to form ternary CS-GO@HKUST-1 xerogel beads, the HKUST-1 MOF structure remained stable for up to two days in a water solution at room temperature, whereas the MOF powder and CS@HKUST-1 xerogel beads underwent significant framework collapse within a day. CO2 adsorption measurements on these xerogel beads also show promising CO2 uptakes, surpassing 2.5 mmol g−1 at 298 K and 1 bar. Moreover, these composites could be regenerated for more than 10 cycles without any loss of quantity adsorbed.

Modeling Mass Transport Dynamics in Deformable Hydrogels during Evaporation.

Hydrogels possess exceptional mechanical properties and biocompatibility, making them widely used in contemporary bioengineering. Specifically, in the development of wearable and implantable health monitoring devices as well as drug delivery systems, hydrogels are utilized to enable precise control over the transport of solutes. Nonetheless, predicting the distribution of substances within hydrogels still poses a significant challenge due to the complex interplay between the movement of water content, migration of solutes, and deformability of the hydrogel polymer network, which presents challenges to theoretical modeling. Our work introduces a numerical model that addresses the movement of water and solute within a flexible hydrogel, accounting for evaporation and/or moisture absorption at the boundary. The model solves for water saturation, solute concentration, and hydrogel deformation iteratively at each time step while computing the boundary movement velocity based on the transport process. By comparing the modeled results of geometry deformation and water and solute distributions during evaporation with our experiments, we demonstrate the accuracy and applicability of our proposed model. This capability to precisely analyze water and solute concentrations in deformable and nonuniform hydrogel environments paves the way for advancements in biosensing and drug delivery methods that rely on elastic porous materials.

Effect of Formation Temperature of Zirconium Dioxide on its Phase Composition and the Efficiency of Adsorptive Removal of Phosphate Anions from a Water Solution

Effect of Formation Temperature of Zirconium Dioxide on its Phase Composition and the Efficiency of Adsorptive Removal of Phosphate Anions from a Water Solution

Industrial circular water use practices through the application of a conceptual water efficiency framework in the process industry

Increased industrial water demand and resource depletion require the incorporation of sustainable and efficient water and wastewater management solutions in the industrial sector. Conventional and advanced treatment technologies, closed-water loops at different levels from an industrial process to collaborative networks among industries within the same or another sector and digital tools and services facilitate the materialization of circular water use practices. To this end, the scope of this paper is the application of the Conceptual Water Efficiency Framework (CWEF), which has been developed within the AquaSPICE project aspiring to enhance water circularity within industries in a holistic way. Four water-intensive process industries (two chemical industries, one oil refinery plant and one meat production plant) are examined, revealing its adaptability, versatility and flexibility according to the requirements of each use case. It is evident that the synergy of process, circular and digital innovations can promote sustainability, contribute to water conservation in the industry, elaborating a compact approach to be replicated from other industries.

Induction of Viable but Non-culturable (VBNC) State in Shigella flexneri Under Osmotic and Nutritional Stresses at Low Temperature

Background: Viable but non-culturable (VBNC) is a specific physiological state in which living bacteria lose the ability to grow and form colonies on conventional bacterial growth media; however, these cells remain metabolically active. Objectives: Considering the importance of the pathogenicity of Shigella flexneri and the possibility of its transmission through contaminated water and food, we aimed to study the possibility of this bacterium entering the VBNC state under osmotic and nutritional stresses at low temperature (4°C). Methods: Shigella flexneri was inoculated in distilled water and NaCl solutions with concentrations of 0, 5, 10, 15, 20, 25, and 30% at 4°C. The cultivability of the bacteria was checked daily. After observing the loss of cultivability, entry into the VBNC state was assessed using RT-PCR, flow cytometry, and fluorescence microscopy. Results: After cultivation of S. flexneri in different concentrations of salt solution, the time of non-cultivability was observed at concentrations of 0, 5, 10, 15, 20, 25, and 30%, respectively, on days 19, 20, 21, 22, 22, 24, and 24. Expression results of ipaH and ipaD genes using RT-PCR, along with the presence of live cells detected by flow cytometry and fluorescent staining, indicated that the cells had entered the VBNC state. Conclusions: Shigella flexneri can survive and enter the VBNC state under nutritional and osmotic stresses at low temperatures (4°C). In this state, although the bacterium is alive, it cannot be detected by conventional culture-dependent methods. Due to the potential risk of bacterial recovery, conventional techniques may be insufficient to detect the presence of pathogens in the VBNC state when evaluating water and food.

Multi-objective optimization and comprehensive Thermodynamic, economic, and environmental analysis of an innovative solar-geothermal integrated system for synergistic power generation and water desalination

ABSTRACT This paper presents a novel multi-objective optimization and sustainability analysis framework for an innovative solar-geothermal integrated system for power generation and water desalination. Harnessing renewable solar and geothermal energy, the system offers a sustainable solution for energy, water, and environmental challenges. Advanced thermodynamic modeling techniques, validated by industry simulations, accurately characterize system performance. Departing from conventional analyses, the research incorporates exergy-based economic and environmental assessments and the emergy concept to quantify the total available energy required, enabling a comprehensive sustainability evaluation. Through multi-objective optimization using genetic algorithms, the system’s design and operational parameters are optimized to enhance exergy efficiency, economic emergy performance, and environmental emergy performance simultaneously. The optimization framework considers turbine inlet conditions, pressures, and desalination configurations to identify optimal operating points balancing energy efficiency, economic feasibility, and environmental impact. Results demonstrate significant improvements of up to 23.49% in exergy efficiency, 25.97% in economic emergy performance, and 16.04% in environmental emergy performance compared to the baseline system. This study focuses on the multi-objective optimization of a novel solar-geothermal integrated system for synergistic power generation and water desalination. The methodology combines thermodynamic, economic, and environmental analyses to evaluate system performance. Key findings include a significant improvement in overall efficiency and sustainability compared to conventional systems, highlighting the potential for large-scale implementation.

Iota-carrageenan as a regenerating system for Eu3+ recovery: adsorption/desorption cycles

ABSTRACT Renewable and biodegradable polysaccharides attract attention as environmentally friendly adsorbents for the removal of heavy metals from wastewater. One such group, is carrageenan, of which were recently successfully employed to adsorb representative lanthanide and actinide ions. Herein, iota-carrageenan-based hydrogels were used to adsorb europium ions (Eu3+) from water solutions, followed by desorption of the ions from the hydrogel beads and recycling of the beads three times. It was found that sorption yields from a 500 mg/L Eu3+ ion solution with beads that were prepared with 1 or 2 wt/v% aqueous solution of iota-carrageenan with CaCl2 (0.5 M) reached maximum sorption yield of 50% and 65%, correspondingly, after 1 h. In addition, the sorption kinetics followed the pseudo second-order model controlled by chemisorption. Desorption yields in the first cycle using NaNO3 (1 M) with both preparations were 57% and 74%, respectively. The sorption yields increased during the second and third cycles and were efficient in the overall pH range. Cryo-SEM, SEM, SEM-EDS and TGA analyses verified the adsorption and desorption of Eu3+ ions to and from the iota beads and that the Ca2+ ions that initially crosslinked the hydrogel were replaced during the cycles by Eu3+ or Na+ ions. In addition, the beads were stable and easily reusable for several sorption/desorption cycles. Furthermore, after sorption, the beads were characterised by a porous structure, such that beads prepared with a 2 wt/v% aqueous solution of iota-carrageenan yielded a more porous, ordered structure, and after desorption, the bead textures became even more porous.