Filtration Of Solution Research Articles

Characterization and evaluation of okra gum as a tablet binder

The type and amount of binders decisively influence the characteristics of tablets prepared by wet granulation procedure. Commonly used binders like acacia, gelatin, starch and hydrolyzed starch have natural origin. The aim of this study was to evaluate the effectiveness of a new binder extracted from Hibiscus esculentus (Okra gum) in tableting. Okra gum was extracted from the pods of Okra fruit by maceration in distilled water followed by filtration of viscous solution as well as precipitation of gum extract by using acetone. To evaluate the binder effectiveness, two models, including a placebo formulation (lactose) and a drug formulation (Acetaminophen, Ibuprofen, and/or Calcium acetate) were evaluated. Granules were prepared by different concentrations (0.5-6 %w/w) of Okra gum and tableted using a Kilian single punch press. Cornstarch (12.5 % w/w) and P.V.P (22 %w/w) were employed as the standard binders for comparison. The physical properties of the granulates and those of the tablets including disintegration time and dissolution rate were studied. The properties of granulates (bulk and tapped density, granule strength, flowability) as well as those of tablets (hardness, friability, disintegration time) were generally good. Moreover, the physical properties of Ibuprofen and Calcium acetate tablets containing Okra gum showed sufficient hardness, desirable disintegration time and low friability. The percent of drug released after 45 minutes were 15 %, 44 % and 96 % for Acetaminophen, Ibuprofen and Calcium acetate tablets, respectively. Okra gum produces some tablet formulations with good hardness and friability. However, this binder prolongs the dissolution rate of some slightly soluble drugs and hence may be good candidate for sustained release formulations. (Symecko C., Rhodes C, et.al.,1995)

Aluminum-Doped Indium Oxide Electron Transport Layer Grown by Atomic Layer Deposition: Highly Efficient and Damage-Resistant Interconnection Solution for All-Perovskite Tandem Solar Cells with 25.46% Efficiency.

In fabricating high-efficiency all-perovskite tandem solar cells (APTSCs) with a p-i-n configuration, the electron transport layer (ETL) plays a critical role in facilitating the transport of photogenerated electrons from the front cell to the recombination layer and protecting the front cell from damage during rear cell fabrication. This study introduces aluminum-doped In2O3 (AIO) films grown by atomic layer deposition (ALD) as a promising ETL for high-efficiency APTSCs. ALD-grown AIO films with an optimized Al concentration exhibit superior charge transport characteristics, excellent transparency, and damage-resistant barrier properties against solution infiltration compared with conventional SnO2 ETLs and undoped ALD In2O3. Using an ALD SnO2/3 at.% AIO bilayer as the electron transport layer, an efficiency of 18.33% is achieved from single-junction wide bandgap perovskite solar cells. Furthermore, the use of ALD SnO2/3 at.% AIO ETL enables the reliable fabrication of APTSCs with negligible solution damage to the front cell and minimized power loss. Consequently, APTSC employing the ALD AIO-based ETL exhibit an excellent photoconversion efficiency of 25.46%, outperforming APTSCs with the ALD SnO2 ETL.

A closed-loop recycling of wastewater derived from aqueous carbonation of basic oxygen furnace slag in cement paste production

Aqueous carbonation (AC) treatment is a promising method for enhancing the cementitious activity of Ca- and Mg-rich solid wastes, such as basic oxygen furnace slag (BOFS), while also reducing carbon emissions. However, the carbonated filtrate (CF) solution generated during the AC process poses significant environmental challenges and limits its large-scale application. This paper, therefore, explores the feasibility of recycling CF in cement paste production as a strategy for managing AC wastewater. The study examines the impact of CF on the physico-mechanical properties, hydration behavior and microstructure of cement pastes (pure and blended with either 10% as-received or carbonated BOFS), compared to those prepared with tap water (TW) and carbonated water (CW). The results indicate that carbonated solutions (CF and CW) promote the hydration of aluminate phase in cement, with a more pronounced effect observed for CW. The solid suspensions in CF, particularly nesquehonite, restrict the growth space for calcium silicate hydrates (C-S-H) in the paste matrix, resulting in the formation of foil-like Type II C-S-H and lowering compressive strength. However, the additional nucleation sites provided by calcite crystals in carbonated BOFS (C-BOFS) accelerate cement hydration in CF-based pastes and mitigate strength loss by promoting the formation of more fibrillary C-S-H. Furthermore, the addition of a superplasticizer reduces interparticle forces in the C-BOFS-CF paste, further enhancing strength development and achieving a 28-day strength comparable to that of the control sample (OPC-TW paste).

A Strategy for Quantifying Microplastic Particles in Membrane Filtration Processes using Flow Cytometry

Microplastic (MP) pollution is ubiquitous in the aquatic environment, with significant quantities of MPs originating from municipal wastewater treatment plants. Efforts to evaluate and implement MP removal processes are underway, with membrane technologies often recommended as an "ideal" solution. A key challenge in evaluating these technologies involves efficiently quantifying MP concentrations in samples. Here, flow cytometry (FC) is demonstrated as an effective technique to obtain concentration measurements of plastic microbeads (MBs; 1-5 μm) suspended in water with/without added humic acid. Regardless of solution conditions, MB concentrations were easily quantified via FC. Subsequently, two microfiltration membranes were challenged to these suspensions. As measured via FC, the 0.45 μm membrane demonstrated effective MB rejection (>99%) whereas the 5 μm membrane exhibited a broad range of rejections (40% to >95%) depending on solution conditions and filtration time. Finally, a model was formulated utilizing FC forward light scattering intensity measurements to estimate MB sizes in samples. Using the model, a 33% reduction in median MB size, on average, was noted across the 5 μm membrane when filtering MBs suspended in humic acid solution, affirming a preferential permeation of smaller particles. Overall, this study advances MP quantification techniques towards validating removal processes.

Solution infiltrated lanthanum nickelate–GDC composite cathode via flash-light sintering for intermediate temperature solid oxide fuel cells

Solid oxide fuel cells (SOFCs) require high operating temperatures to minimize the oxygen reduction reaction resistance at cathode and increase the ionic conductivity of oxygen. However, at high operating temperatures, their stability during long-term operation degrades because of material deterioration and the mutual chemical reactions occurring at the interfaces. Herein, an electrode–electrolyte composite is fabricated by solution infiltration of lanthanum nickelate (LNO) electrode material into a GDC electrolyte layer to ensure more reaction sites compared with the conventional powder mixing of the electrode and electrolyte material. Further, the conventional thermal sintering process is replaced with the flash-light sintering process. Thus, the performance of the LNO–GDC cathode cell manufactured by flash-light sintering improves owing to suppression of grain growth of the infiltrated LNO particles. The microstructures of the infiltrated solution and composite layer of the electrolyte material are analyzed using field-emission scanning electron microscopy, and the crystallinity of the LNO nanoparticles is analyzed using high-resolution transmission electron microscopy. A maximum power density of 1.1 W/cm2 is achieved, an improvement of 58 % over the LSCF cell without infiltration at 750 ℃. This study is expected to contribute to the commercialization of SOFCs by replacing conventional thermal sintering.

Prediction and investigation of water repeated absorption and release properties of superabsorbent polymers during the dry-wet cycles in different solutions

Superabsorbent polymers (SAP) with a three-dimensional cross-linked network structure are used in the concrete field due to their good water absorption and water retention properties. The changes of its repeated water absorption and release properties have an important impact on crack healing, but there is still a lack of relevant research. This study mainly uses the tea-bag method to explore the repeated water absorption and release behavior of sodium polyacrylate and polyacrylic acid-acrylamide copolymers in deionized water, cement filtrate, and saturated calcium hydroxide solution. The quantitative analysis of the change in the peak area of the water-absorbing functional group was performed by fourier transform infrared spectroscopy. The morphology and elements of SAP under different dry-wet cycles were analyzed by scanning electron microscope-energy spectrum analysis. The repeated swelling behavior of SAP was predicted using the classical models. The results showed that the repeated water absorption performance of SAP gradually decreased with the increase of the number of wet-dry cycles. The slope of the curve for the second-order equation gradually increases, and the peak area corresponding to the carboxyl functional group also gradually increases. And the rate and amount of water release gradually increase. For sodium polyacrylate, with the increase in the number of wet-dry- cycles, the increase in the content of calcium, magnesium, and aluminum elements is accompanied by a significant decrease in the content of sodium elements. In contrast, the calcium content on the surface of polyacrylic acid-acrylamide copolymer increased, but the sodium content only slightly decreased.

Enhancing the mechanical performance of 3D-printed self-hardening calcium phosphate bone scaffolds: PLGA-based strategies

Over the last decade, 3D-printed porous calcium phosphates have emerged in the market for customized bone reconstruction. However, despite their excellent biological properties, the inherent brittleness is an obstacle that limits their clinical applications, as the scaffolds must withstand the surgical procedures and the mechanical stresses once implanted. Low-temperature self-hardening calcium phosphate inks offer unique possibilities to be reinforced with polymers, as they do not require high-temperature treatments. This study compares two routes for incorporating poly (lactic-co-glycolic acid) (PLGA) into 3D-printed calcium phosphate scaffolds: i) the use of a PLGA solution as a binder in an alpha-tricalcium phosphate self-hardening ink; ii) the infiltration of a PLGA solution into previously hardened 3D-printed calcium-deficient hydroxyapatite scaffolds. The influence of the added PLGA on the physical-chemical properties, mechanical performance and in vitro biological properties is assessed using a commercially available biomimetic calcium phosphate scaffold as a control. The addition of PLGA increases the plastic deformation capacity and the strength, both in compression and bending, and significantly improves the work of fracture of the scaffolds, up to an 8-fold in compression when PLGA is incorporated as a binder in the ink. Moreover, screwability tests demonstrate the enhanced fixability of the composite scaffolds in a knife-edge ridge indication with challenging fixation in the jaw. Importantly, the improvement of the mechanical properties by the addition of PLGA does not impair the good cytocompatibility of the material. Regarding the two routes studied, the PLGA incorporation in the ink is the best option in terms of overall improvement of the mechanical performance and osteogenic cell response.

MXene/MWCNTs-based capacitive pressure sensors combine high sensitivity and wide detection range for human health and motion monitoring

Wearable pressure sensors with exceptional performance are playing a crucial role in various fields such as electronic skin, human motion monitoring, medical diagnosis, and human-computer interaction. However, achieving both high sensitivity and a wide sensing range with simple fabrication and low cost has proven to be a significant challenge for sensors. In this study, a simple capacitive pressure sensor is proposed that multi-walled carbon nanotubes (MWCNTs) are introduced into MXene (Ti3C2TX) as a ‘bridge’. Then the electrode which has excellent conductivity is obtained by filtration of MXene solution and MXene/MWCNTs solution at intervals. Additionally, green and degradable cellulose paper is used as the dielectric layer. The fabricated pressure sensor exhibits a high sensitivity of 4.7 kPa−1 for low pressure from 0 to 1 kPa, a wide detection range of 0–700 kPa, ultra-fast response and recovery times of 46 ms and 62 ms, respectively, and an extremely low detection limit of 0.32 Pa. The sensor remains stable even after 4500 cycles and can accurately monitor the movement of the human joints. Furthermore, it can track human physiological signals, which is beneficial for medical diagnosis and disease prevention, and has significant potential for application in the wearable technology field.

Enhancing biocementation performance in low permeability clayey soil through sand column strategy

Soil erosion is a common phenomenon which causes lots of geological and engineering disasters. Clayey soil erosion control is a hot research topic and a challenging issue for its low permeability and lack of effective infiltration of treatment solutions. In this study, a coupling microbially induced calcium carbonate precipitation (MICP)-sand column method was proposed as a promising and sustainable technique to mitigate surface clayey soil erosion with adjustable treatment depth. Seven groups of soil samples were prepared, including pure soil, MICP-treated soil, and MICP-sand column method-treated soil. A series of disintegration tests and penetration tests were conducted to investigate the method feasibility and adjusting mechanism of erosion mitigation with varying sand column heights and diameters. Compared to pure soil sample, sample treated by MICP-sand column (6 cm-height and 3 cm-diameter) method could reach a maximum reduction of 50 % in ultimate disintegration rate and a 30 % increase in the highest penetration resistance. The sample has a 7.9 cm effective treatment depth, which is 5.3 times of the MICP-treated sample. The mechanism of erosion mitigation can be attributed to that the sand column serves as a favorable path for the bacteria suspension and cementation solution in low-permeability-clayey soil and improves the effective depth of MICP treatment. Adjusting the height and diameter of sand column can change the calcium carbonate distribution, especially at the locations near the surface and around the sand column. In this study, the optimal height and diameter are 6 cm and 3 cm, respectively, and finally form a U-shape three-layer structure. The structure significantly increases the proportion of the hard crust layer and weak-cemented layer with high hydro-mechanical properties. In conclusion, the coupling MICP-sand column method with reasonable height and diameter of sand column shows the ability to control surface erosion of soil and has better long-term mitigation performance.

Facile infiltration of polyethyleneimine as a strong CO2 retardant in scalable dual-polymer membranes for H2/CO2 separation

Successful pre-combustion CO2 capture from synthetic gas for H2 production requires effective membrane separation technology. While polymer-based membrane materials offer promising industrial scalability, they generally lack a sufficiently high H2/CO2 selectivity to make this process energy-efficient. In this work, we have designed a scalable dual-polymer blend membrane consisting of sulfonated polyphenylsulfone (sPPSU) and polybenzimidazole (PBI), and then being infiltrated with amine-rich poly(ethyleneimine) (PEI) molecules as effective CO2 retardants to substantially elevate the H2/CO2 selectivity. PEI molecules were infiltrated into the dual-polymer matrix via solution-treatment to crosslink the polymer network and retard CO2 transport using its amine-rich nature. The PEI infiltration dramatically increased the H2/CO2 selectivity of the dual-polymer matrix from 4.6 to up to 59.3 while maintaining a minimum H2 permeability of 2.49 Barrer at a low temperature of 35 °C, which not only surpasses the Robeson upper bound but also places the newly developed membrane among the best-performing polymer-based membranes. More importantly, the solution infiltration of PEI incurs no phase segregation, maintaining the polymer mechanical robustness, which is crucial for industrial scaling. This study offers promising opportunities to develop three-polymer membrane systems for H2/CO2 separation using synergistic polymer blends and CO2-retarding molecules.

Multiple heteroatom-doped cobalt sulfoselenide@C yolk-shell microsphere as excellent anode materials for sodium-ion batteries and their conversion reaction mechanism with sodium ions

To address the sluggish reaction kinetics commonly associated with the transition metal chalcogenide anodes in their interaction with alkali metal ions, introducing heterostructures into these materials is proposed as a novel approach. Herein, we introduce a fabrication method for yolk-shell structured microsphere comprising heteroatom-doped cobalt sulfoselenide nanocrystals using a recycled solution. The prepared material demonstrates a composition of sulfur-doped cobalt selenide, forming hetero-anion metal compounds. A detailed study of the reaction mechanism in cobalt sulfoselenide reveals the formation of Na2S/Na2Se heterointerfaces during the conversion reaction, which facilitate a rapid diffusion of Na-ions. Furthermore, heteroatom doping in the cobalt sulfoselenide nanocrystals, induced by cobalt recycling process, leads to the lattice expansion, further enhancing the Na-ion diffusion kinetics. Additionally, through an infiltration of pitch solution and a simple heat-treatment, pitch-derived carbon is coated on the cobalt sulfoselenide nanocrystals. This carbon layer can effectively accommodate the volumetric stress during repeated cycling, enhancing the stability. Consequently, carbon-coated heteroatom-doped cobalt sulfoselenide yolk-shell microsphere anode exhibits stable cycling stability (560 mA h g−1 for 100 cycles at 0.2 A g−1) as well as great rate capability (140 mA h g−1 at 15 A g−1) for sodium-ion batteries (SIBs).

A green zwitterionic bi-continuous membranes prepared by dual-bath procedure for mitigating biofouling during bacterial removal from water

This work explores the possibility of forming green microfiltration antifouling membranes based on polyvinylidene fluoride (PVDF) and a zwitterionic copolymer derivative of sulfobetaine methacrylate (SBMA), utilizing gamma-valerolactone (GVL) as the solvent and a mixture of ethanol and water as non-solvents. Efforts were initially focused on adjusting the immersion time of the matrix polymer in alcohol alone to obtain a porous structure, and 15 s were sufficient to achieve a symmetric, open porous morphology. Next, the polymer/copolymer/solvent blend was characterized. While it did not show the characteristics of a fully miscible system, DLS and visual observations revealed the obtaining of a homogeneous (relatively narrow particle size) and transparent to translucent system. Thus, membranes could be cast, and were shown to be stable. The addition of the copolymer maintained the physical characteristics of microfiltration membranes, but an FT-IR analysis revealed its effect on the dominant crystalline polymorph (switching from β to α). The membrane wettability was enhanced in an important extent with a dynamic water contact angle (WCA) gradually falling to < 40° (while the virgin membrane's WCA remained about 138° all test long), and a hydration capacity reaching about 530 mg/cm3 against <10 mg/cm3 for the virgin membrane. It reflected on the antifouling abilities of the membranes as tested using bovine serum albumin, fibrinogen, Escherichia coli, and Stenotrophomonas maltophilia, with relative decreases in adsorption during static tests measured to be 95 %, 70 %, 91 % and 98 %, respectively. Finally, compared to the virgin membrane, the modified membrane featured improved flux recovery (32 % vs. 11 %), significantly higher rejection (98.9 % vs. 89.1 %) and lower irreversible fouling tendency (68 % vs. 89 %) during cyclic water/bacterial solution filtration in dead-end mode, making it potentially suitable for addressing bacterial pollution in wastewater.

Kinetic study of reaction formation of phosphate products from thermal dissolution of wolframite using fusion technique

This study examined an alternative technique of extracting tungsten from wolframite ore using a fusion method with ammonium phosphate salt. Current techniques use alkali salts to decompose tungsten ores and use various purification methods to produce ammonium paratungstate, which is a key intermediate precursor in the extraction of tungsten. In this study, a two-step extraction process, which involves thermal decomposition of the ore using fusion and a separation stage, is examined. The novelty of this technique is the ability to completely decompose wolframite ore and form an unstable tungsten oxide phosphate (WO2(PO3)2) compound. The instability of WO2(PO3)2 in deionized water enables selective isolation of tungsten as insoluble precipitates of WO3 and WO2. The decomposition reaction of WO2(PO3)2 is influenced by the presence of oxygen and determined to be first order under ambient conditions. Scanning electron micrographs and X-ray diffraction analysis showed above 80% of the tungsten precipitated compared with the amount that remained in the filtrate solution.

Polyetherketoneketone/carbon fiber composites with an amorphous interface prepared by solution impregnation

Interfacial adhesion between carbon fibers (CF) and polyetherketoneketone (PEKK) is a key factor that affects the mechanical performances of their composites. It is therefore of great importance to impregnate the CF bundles with PEKK as efficiently as possible. We report that PEKK with a good dispersion in a mixed solution of 4-chlorophenol and 1,2-dichloroethane can be introduced onto CF surfaces by solution impregnation and curing at 280, 320, 340 and 360 °C. The excellent wettability or infiltration of the PEKK solution guarantees a full covering and its tight binding to CFs, making it possible to evaluate the interfacial shear strength (IFSS) with the microdroplet method. The interior of the CF bundles is completely and uniformly filled with PEKK by solution impregnation, leading to a high interlaminar shear strength (ILSS). The maximum IFSS and ILSS reached 107.8 and 99.3 MPa, respectively. Such superior shear properties are ascribed to the formation of amorphous PEKK in the small spaces between CFs.

Synergistic Leaching of Titanium, Aluminum, and Magnesium Components during Dilute Acid Pressure Treatment of High-Titanium Blast Furnace Slag.

This study focuses on an improved leaching process through the combination of pressurized conditions and direct filtration of acid leaching slurry, which is conductive to improving the filterability of acid leaching systems and the extraction rates of Ti, Al, and Mg components. The effects of sulfuric acid concentration, reaction temperature, particle size of materials, acid-slag ratio, and reaction time on the leaching efficiency were systematically investigated. The results showed that pressurization significantly enhances the filtration efficiency of the reaction slurry. Under the same filtration time, the filtration efficiency increased from 46% under ordinary pressure to 78% under pressurized conditions. Moreover, under the optimal reaction conditions, the extraction rates of Ti, Al, and Mg components were more than 88.21%, 97.8%, and 96.31%, respectively. Additionally, XRD and FTIR showed that titanium oxide sulfate hydrate crystals were produced in the acid-leached residues when the reaction temperature exceeded 190 °C, thereby reducing the extraction rate of Ti component. And the XRD pattern shows that when the reaction temperature is maintained at 190 °C and the reaction time is extended to 150 min, titanium oxide sulfate hydrate crystals will be formed to reduce the extraction rate of the Ti component. In summary, this study not only provides important theoretical support for the resource utilization of high-titanium blast furnace slag but also offers a feasible solution for efficient extraction and convenient filtration, thus holding significant academic and practical implications.

Unlocking the potential of zwitterionic vapor-induced phase separation membranes synthesized from maleic anhydride in polyvinylidene fluoride-based systems for antifouling applications

This work presents an approach to form zwitterionic porous poly(vinylidene fluoride) (PVDF) membranes fabricated by vapor-induced phase separation (VIPS). The reaction between maleic anhydride groups, incorporated initially in the casting solution by blending styrene maleic anhydride (SMA), with 3-((3-aminopropyl)dimethylammonio)propane-1-sulfonate led to the desired zwitterionic moieties. XPS and FTIR analyses confirm the functionalization of the membrane. SEM analyses revealed that it did not have any major impact on the membrane morphology deemed to be close to bicontinuous. While the mean pore size of the virgin membrane was 0.57 μm, it increased to 0.85 μm suggesting the pore-forming effect of SMA during the phase-inversion process. Hydration was significantly enhanced, attributed to the zwitterionic groups on the one hand, but also to the formation of carboxylic acid and amide groups following the ring-opening reaction. It led to significant resistance to bacterial attachment as tested with 4 strains of bacteria including Escherichia coli, Stenotrophomonas maltophilia, Staphylococcus aureus and Streptococcus mutans (>99 % reduction for each). Applied in cyclic water/bacterial solution filtration tests, the modified membrane showed clear improvement in overall performances. Hence, for the virgin membrane, the initial water permeability, flux recovery ratio after the first cycle and flux recovery ratio after the second cycle were found to be 3000 L m−2 h−1.bar−1, 12 % and 53 %, respectively. For the optimized zwitterionic membrane, they were measured to be 7000 L m−2 h−1.bar−1, 26 % and 100 %, respectively. The efficacy of styrene maleic anhydride as a precursor for achieving stable and efficient zwitterionization of PVDF microfiltration membranes is evidenced, rendering it valuable for the filtration of microorganism-containing wastewater. Moreover, its potential application extends to the biomedical realm.

Investigation on ion concentration of pore water in compacted bentonite after infiltrated by salt solutions

The behavior of salt solutions infiltrated into compacted bentonite was investigated in this study, with particular attention paid to the ion concentration in the pore water, in order to improve the understanding of the bentonite behavior in geological disposal projects. A Japanese bentonite, Kunigel V1 (K_V1), was used to prepare specimens with a thickness of 2 mm and an initial dry density of 1.4 to 1.7 Mg/m3. For each density case, salt solutions (NaCl, KCl, and CaCl2) of different amounts (0 to 2 mol/L) were supplied to the specimens. After infiltration, the basal spacing (d001) and exchangeable cations of the montmorillonite in the bentonite and the leached cations from the bentonite were measured. Based on the test results, the ion concentration in the interlayer pore water of the montmorillonite or the interparticle pore water was discussed. The findings indicated that the infiltration capacities of the various salt solutions into the compacted K_V1 bentonite were in the order of KCl > CaCl2 > NaCl. The K_V1 specimen with the highest initial dry density exhibited the strongest resistance to salt solution infiltration. After the infiltration of the NaCl solution into the compacted K_V1 bentonite, the increased sodium ions mainly remained in the interparticle pores, leading to an increase in the sodium ion concentration in the interparticle pore water. During the infiltration of the KCl and CaCl2 solutions into the compacted K_V1 bentonite, the infiltrated potassium ions in the case of KC1 and the calcium ions in the case of CaCl2 tended to penetrate the interlayer pore preferentially, thereby displacing the exchangeable sodium ions. After most of the exchangeable sodium ions that had initially existed in the montmorillonite had been replaced, the infiltrated potassium or calcium ions remained in the interparticle pores.

Hormone replacement therapy did not alleviate temporomandibular joint inflammatory pain in ovariectomized rats.

This study had the aim of examining the relationships between variations in estrogen levels resulting from ovariectomy, and estrogen hormone replacement therapy (HRT) in rats subjected to an orofacial inflammatory pain model. Eighty adult female Wistar rats were initially divided into 2 groups: Sham or ovariectomy (OVX-D1). Seven days later (D7), the rats were subjected to an unilateral infiltration of Freund's Complete Adjuvant (CFA) or saline solution into the right temporomandibular joint (TMJ). Then, rats received 17β-estradiol (28µg/kg/day) or placebo for 21days (D10-D31). Nociception was evaluated by the von Frey (VF) and the Hot Plate (HP) tests, and depressive-like behavior by the Forced Swimming (FS) test. On D32 all rats were euthanized and serum, hippocampus and brainstem were collected. The CFA groups presented a mechanical hyperalgesia until day 21 (p ≤ 0.05). No differences were observed among groups in the HP (p = 0.735), and in the immobility and swimming time of the FS (p = 0.800; p = 0.998, respectively). In the brainstem, there was a significant difference in the TNF-ɑ levels (p = 0.043), and a marginal significant difference in BDNF levels (p = 0.054), without differences among groups in the hippocampal BDNF and TNF-ɑ levels (p = 0.232; p = 0.081, respectively). In conclusion, the hormone replacement therapy did not alleviate orofacial pain in ovariectomized rats. However, there is a decrease in brainstem TNF-ɑ levels in the animals submitted to both models, which was partially reverted by HRT.

STUDYING THE EFFECTIVENESS OF CERAMIC MEMBRANES IN FILTERING PHARMACEUTICALS

This study assessed the effectiveness of ceramic membranes in removing drugs from water. The effectiveness was assessed by filtration of model solutions with the addition of sulfamethoxazole and aspirin at a concentration of 3 mg/l. The study of drug concentrations was carried out using high-performance liquid chromatography (HPLC). The results showed 100% and 99.48% removal of aspirin and sulfamethoxazole from the solution, respectively. When filtering model solutions with the addition of medicinal substances, a decrease in the flow of solutions was observed over time and amounted to 19 l/m2-h for sulfamethoxazole and 30 l/m2-h for aspirin, respectively. Overall, the results obtained indicate that ceramic membranes have the potential to purify water from medicinal contaminants.

Investigating the Impact of Superabsorbent Polymer Sizes on Absorption and Cement Paste Rheology.

This study aims to understand the water retention capabilities of Superabsorbent Polymers (SAPs) in different alkaline environments for internal curing and to assess their impact on the rheological properties of cement paste. Therefore, the focus of this paper is on the absorption capacities of two different sizes of polyacrylic-based Superabsorbent Polymers : SAP A, with an average size of 28 µm, and SAP B, with an average size of 80 µm, in various solutions, such as pH 7, pH 11, pH 13, and cement filtrate solution (pH 13.73). Additionally, the study investigates the rheological properties of SAP-modified cement pastes, considering three different water-to-cement (w/c) ratios (0.4, 0.5, and 0.6) and four different dosages of SAPs (0.2%, 0.3%, 0.4%, and 0.5% by weight of cement). The results showed that the absorption capacity of SAP A was higher in all solutions compared to SAP B. However, both SAPs exhibited lower absorption capacity and early desorption in the cement filtrate solution. In contrast to the absorption results in pH 13 and cement filtrate solutions, the rheological properties, including plastic viscosity and yield stress, of the cement paste with a w/c ratio of 0.4 and 0.5, as well as both dry and wet (presoaked) SAPs, were higher than those of the cement paste without SAP, indicating continuous absorption by SAP. The viscosity and yield stress increased over time with increasing SAP dosage. However, in the mixes with a w/c ratio of 0.6, the values of plastic viscosity and yield stress were initially lower for the mixes with dry SAPs compared to the reference mix. Additionally, cement pastes containing wet SAP showed higher viscosity and yield stress compared to the pastes containing dry SAP.