Kinetic Rate Research Articles

Performance analysis of an underwater wireless optical communication link with Lommel beam

Abstract In order to mitigate the stochastic interference of underwater channels and improve the quality of underwater communication systems, it is essential to study the performance of the underwater wireless optical communication (UWOC) links utilizing vortex beams with unique attributes. In this paper, the analytical formulae for the bit error rate (BER) and the average capacity of the UWOC link with diffraction-free Lommel beam are derived under the Rytov theory. Simulation results demonstrate that the system with a long wavelength, a high system signal-to-noise ratio(SNR), a small asymmetric parameter and receiving aperture diameter achieves a high average capacity and a low BER. Furthermore, in the underwater channel with a larger kinetic energy dissipation rate per unit mass of fluid and inner scale, a smaller mean-squared temperature dissipation rate, temperature salinity contribution ratio and transmission distance, the performance of the communication link can be improved. Meanwhile, it is found that the performance of the link with carrier Lommel beam are less sensitive to the topological charge, the scaling factor of the beam and the turbulent outer scale. These findings provide theoretical support for the design and implementation of an UWOC link utilizing the Lommel beam.

Methane Combustion Kinetics over Palladium-Based Catalysts: Review and Modelling Guidelines

Fugitive methane emissions account for a significant proportion of greenhouse gas emissions, and their elimination by catalytic combustion is a relatively easy way to reduce global warming. New and novel reactor designs are being considered for this purpose, but their correct and efficient design requires kinetic rate expressions. This paper provides a comprehensive review of the current state of the art regarding kinetic models for precious metal catalysts used for the catalytic combustion of lean methane mixtures. The primary emphasis is on relatively low-temperature operation at atmospheric pressure, conditions that are prevalent in the catalytic destruction of low concentrations of methane in emission streams. In addition to a comprehensive literature search, we illustrate a detailed example of the methodology required to determine an appropriate kinetic model and the constants therein. From the wide body of literature, it is seen that the development of a kinetic model is not necessarily a trivial matter, and it is difficult to generalize. The model, especially the dependence on the water concentration, is a function of not only the active ingredients but also the nature of the support. Kinetic modelling is performed for six catalysts, one commercial and five that were manufactured in our laboratory, for illustration purposes.

Evaluating and modeling the efficacy of Stipagrostis plumosa for the phytoremediation of petroleum compounds in crude oil-contaminated soil

ABSTRACT This study focused on using Stipagrostis plumosa for phytoremediation to eliminate total petroleum hydrocarbons (TPHs) and heavy metals (HMs) like cadmium (Cd), chromium (Cr), lead (Pb), and nickel (Ni) from oil-contaminated soil. Conducted over six months at a field-scale without artificial pollutants, soil samples were analyzed using gas chromatography‒mass spectrometry (GC‒MS) for TPHs and inductively coupled plasma-optical emission spectroscopy (ICP‒OES) for HMs. Results after six months revealed that plots with plants had significantly higher average removal percentages for TPHs (61.45%), Cd (39.4%), Cr (46.1%), Pb (41.5%), and Ni (44.2%) compared to the control group (p <0.05). Increased microbial respiration and bacteria populations in planted plots indicated enhanced soil microbial growth. Kinetic rate models aligned well with the first-order kinetic rate model for all pollutants (R2 >0.9). Overall, the study demonstrates that S. plumosa can effectively reduce TPHs and HMs in oil-contaminated soil, making it a promising option for pollutant absorption.

Green synthesis and photocatalytic proficiency of tunable SnO2 nanostructures: unveiling environmental-friendly strategies for sustainable water remediation

Abstract This study demonstrates a proficient and eco-friendly synthesis of SnO2 nanostructures using a hydrothermal method, without the requirement of extra surfactants. The synthesis was systematically performed by adjusting the molar ratio of stannic chloride to sodium hydroxide and varying the pH settings. It was noted that the pH value rises according to the concentration of sodium hydroxide. A comprehensive analysis was performed to characterize the resulting nanostructures, which involved studying their structural features, chemical composition, morphology, and optical properties. An X-ray diffraction (XRD) analysis showed that increasing the pH values resulted in a noticeable improvement in the crystalline structure and a decrease in the density of surface defects. The SnO2 nanostructures, synthesized using different pH settings, were subsequently assessed for their photocatalytic performance in the degradation of methylene blue (MB) dye under simulated solar irradiation. Surprisingly, the nanostructure produced at higher pH levels showed outstanding results, as 97% of the dye was broken down in just 70 minutes when exposed to simulated solar radiation. The analysis uncovered a maximum rate constant (k) value of 0.04 min−1, determined using pseudo first-order rate kinetics. In order to better understand the photodegradation process, scavenger experiments were performed to identify the active species involved. These investigations provided valuable insights into the complex mechanisms that drive the observed photocatalytic activity. This study not only enhances the progress of SnO2 nanostructures but also highlights their potential as strong and environmentally friendly materials for effective photocatalytic applications.

Highly efficient electrocatalysis of oxygen to hydroxyl radical by FeN2O2 single-atom catalyst for refractory organic pollutant removal

The heterogeneous electro-Fenton (Hetero-EF) provides an effective and environmentally friendly method for refractory pollutants removal by strongly oxidative •OH. However, the •OH generation shows an insufficient activity in activating H2O2 to •OH due to the too strong H2O2 binding on the catalytic site. Here, an iron single-atom FeN2O2 catalyst anchored on hollow spherical porous carbon (FeN2O2-HPC) was designed to enhance •OH production by modulating the H2O2 binding. The FeN2O2-HPC Hetero-EF system showed a •OH production rate of 25.0 μmol h−1 and kinetic rate constant of 2.06 h−1 for phenol removal, which exceeded the FeN4 catalyst (the most reported iron single-atom). Density function theory calculations revealed that FeN2O2 could lower the H2O2 adsorption energy and energy barrier of H2O2 activation to •OH compared with FeN4, thus enhancing •OH production. This work gives a new insight into the •OH generation enhancement of Hetero-EF by modulating single-atom coordination environment for refractory pollutants removal.

Combustion performance of hydrogen fueled parallel wall-jet used for drag reduction in a supersonic combustor

Hydrogen fueled parallel wall-jet combustion is considered to be one of the most promising drag reduction technologies in supersonic combustors, researchers mainly focus on its drag reduction mechanism, while balancing its combustion efficiency and drag reduction performance is of great significance for engine performance and energy conservation. In this paper, combustion performance of hydrogen fueled parallel wall-jet is numerically investigated. Kinetic reaction rate and scalar dissipation rate are defined to decouple the chemical reaction and mixing processes. Results indicate that although hydrogen fueled parallel wall-jet combustion is a nonequilibrium chemical reaction process, the combustion process is dominated by mixing due to the much larger magnitude order of kinetic reaction rate. The investigation also reveals that, compared to the effects of mainstream total temperature, mainstream Mach number presents a more significant effect on combustion efficiency. Moreover, combustion efficiency increase first brings negative and then brings beneficial effects on drag reduction performance, which is due to the different sensibilities of the two skin friction determinants viscosity and velocity gradient to combustion efficiency. It is found that, viscosity is more sensitive to combustion efficiency, with combustion efficiency increases by 5.4 %, viscosity increases by 4.15 %, while velocity gradient only decreases by 2.19 %.

Preparation and electrocatalytic oxygen evolution of bimetallic phosphates (NiFe)2P/NF

Abstract The energy and environmental crisis pose a great challenge to human development in the 21st century. The design and development of clean and renewable energy and the solution for environmental pollution have become a hotspot in the current research. Based on the preparation of transition metal phosphates, transition metals were used as raw materials, Prussian blue-like NiFe(CN)6 as a precursor, which was in situ grown on nickel foam (NF) substrate. After low temperature phosphating treatment, a bimetallic phosphide electrocatalyst (NiFe)2P/NF was prepared on NF substrate. Using 1 mol·L−1 KOH solution as a basic electrolyte, based on the electrochemical workstation of a three-electrode system, the electrochemical catalytic oxygen evolution performance of the material was tested and evaluated. Experiments show that (NiFe)2P/NF catalyst has excellent oxygen evolution performance. In an alkaline medium, the overpotential required to obtain the catalytic current density of 10 mA·cm−2 is only 220 mV, and the Tafel slope is 67 mV·dec−1. This is largely due to: (1) (NiFe)2p/NF nanocatalysts were well dispersed on NF substrates, which increased the number of active sites exposed; (2) the hollow heterostructure of bimetallic phosphates promotes the electron interaction between (NiFe)2P and NF, increased the rate of charge transfer, and the electrical conductivity of the material is improved; and (3) theoretical calculations show that (NiFe)2P/NF hollow heterostructure can effectively reduce the dissociation barrier of water, promote the dissociation of water; furthermore, the kinetic reaction rate of electrocatalytic oxygen evolution is accelerated. Meanwhile, the catalyst still has high activity and high stability in 30 wt% concentrated alkali solution. Therefore, the construction of (NiFe)2P/NF electrocatalysts enriches the application of non-noble metal nanomaterials in the field of oxygen production from electrolytic water.

Revealing the inhomogeneous nature of microstructure and texture evolution in the cold-rolled CoCrFeMnNi alloy during static recrystallization

In the present investigation, equiatomic CoCrFeMnNi high entropy alloy (HEA) was subjected to 80% cold rolling (as-rolled) followed by isothermal annealing treatment at 700 °C for different time periods. Microstructural characterization was performed using electron back-scattered diffraction (EBSD) and electron channeling contrast imaging (ECCI) techniques on the as-rolled and annealed samples. The as-rolled microstructure consisted of elongated grains mainly composed of strong α-fiber and weak γ-fiber textures. The as-rolled sample showed the formation of ingrain SBs in the γ-fiber grains, which served as preferential sites for grain nucleation. The annealing treatment of as-rolled samples at 700 °C cause static recovery (SRV) before 5 minutes of heat-treatment, whereas static recrystallization (SRX) was observed after 5 minutes of heat-treatment in the CoCrFeMnNi alloy samples. A faster rate of recrystallization kinetics was observed after 15 minutes of heat-treatment. The annealing treatment reduced the intensity of α-fiber and enhanced the Copper, Cube and P ({011}<122>) texture components. Copper components originated from coarse recrystallized grains, which were the results of localized grain growth phenomena. Unusual behavior of banded featured α-fiber grains was observed during the annealing process. These banded grains in the partially annealed samples consisted of subgrain-boundaries and showed a delayed response to recrystallization as compared to grains with other orientations. Stored energy (SE) and Taylor factor (M) calculations were also used to understand the delayed recrystallization response of the banded featured/retained deformed grains. The microhardness value of the as-rolled sample was approximately 450 Hv, which decreased to around 230 Hv for the fully recrystallized grains.

Facile ligand-regulated synthesis of defective Fe-MOF nanosheets for efficient tetracycline degradation via photoassisted enhanced activation of persulfate

In this work, defective Fe-based metal organic framework (Fe-MOF) were synthesized by a simple and eco-friendly method, in which the benzenetricarboxylic acid (BTC) ligand was partially replaced by cheap terephthalic acid (TPA) to regulate the crystalline morphology, pore structure and ligand defects. At BTC/TPA = 5/3, 4/4 and 3/5 (molar ratio), lamellar crystal (1-Fe-MOF), a mixture of lamellar crystal and nanosheets (2-Fe-MOF), and nanosheets (3-Fe-MOF) were obtained, respectively, which were distinctly different from the octahedral Fe-MOF. In the visible-light-driven persulfate (PS) activation coupled system, 3-Fe-MOF exhibited highest catalytic activity for tetracycline hydrochloride (TCH). 96.5% of TCH was removal within 20 min and the degradation kinetics rate of 0.144 min−1 was 3.5 times higher than that over the intact Fe-MOF. The enhancement in degradation activity was mainly attributed to the emergence of mesoporous structure, exposure of more metal active sites, and accelerated Fe2+/Fe3+ cycling due to more efficient charge separation and electron transfer efficiency, which favored the generation and dominant role of ∙SO4− in TCH degradation. Furthermore, demethylation, deamidation, double-bond oxidation and ring-opening reactions were inferred as the two possible degradation pathways of TCH in 3-Fe-MOF/PS/Vis system. This study provides useful guidance for the design of novel and sustainable MOFs with good application performance and industrialization potential.

Separation of kinetic rate orders in extreme ultraviolet transient grating spectroscopy

We present an extreme ultraviolet (EUV) transient grating (TG) experiment of the spinel Co3O4 compound using tuneable incident energies across the Co M2,3-edge and a 395 nm probe pulse, detecting both the first and the second diffraction orders (SDOs). While the first diffraction order shows a monotonous behavior as a function of time, with a sharp response at t = 0, followed by a weak sub-picosecond component and a nearly constant signal thereafter, the time dependence of SDO varies dramatically with the incident energy as it is tuned across the Co M-edge, with the appearance of a component at t > 1 ps that grows with increasing energy. The results are rationalized in terms of the deviations of the initial grating from sinusoidal to non-sinusoidal, namely a flattening of the grating pattern, that introduces new Fourier components. These deviations are due to higher order, three-body terms in the population relaxation kinetics. The present results highlight the use of the SDO response in EUV TG as a tool to identify higher order terms in the population kinetics.

A one-dimensional diffusive transport model to evaluate H2S generation in salt caverns hydrogen storage sites

Salt caverns are considered a potential hydrogen storage site given the ductility, tightness, and chemical inertness of halite. In addition, unlike porous media, salt caverns require less cushion gas and allow more cycles of injection and production within a year. However, hydrogen is an electron donor for many hydrogenotrophic microorganisms including halophilic sulfate-reducing microbes (SRM) and hydrogen sulfide (H2S) can be generated in a cavern once sulfate and hydrogen become available in the aqueous phase. As salt deposits are often associated with large amounts of impurities such as anhydrite and gypsum, their dissolution during the leaching phase can release the required sulfate ions for SRMs to produce H2S once hydrogen diffuses and dissolves in the brine at the bottom of the cavern. In this study, a one-dimensional diffusive transport model was developed using PHREEQC to simulate sulfate reduction and H2S generation in a cavern at the gas-brine interface. The solution of Fick's diffusion equation was used to calculate the hydrogen concentration at each level of the 1D model while the kinetic rates of reactions were derived from reported experimental and field site observations of brine samples taken from salt caverns. The results obtained indicated that hydrogen consumption at the gas-brine interface can trigger H2S and methane formations. This is followed by a reduction in sulfate and carbonate concentration and a slight increase in pH due to the reduction of protons in the solution. It was also observed that the presence of Fe2+ ions can reduce the amount of the hydrogen sulfide production while Ca2+ ions slightly favour sulfate reduction due to the production of methane. Although the kinetic reaction rate of the reactions in the model is subject to a certain degree of uncertainty, the workflow and results this study can serve as a guide for the future storage of hydrogen in salt caverns.

Freezing-enhanced degradation of azo dyes in the chloride-peroxymonosulfate system

In this study, we investigated the freezing-induced acceleration of dye bleaching by chloride-activated peroxymonosulfate (PMS). It has been observed that the oxidation of chloride by PMS generates a free chlorine species, such as hypochlorous acid (HOCl), under mild acidic and circumneutral pH condition. This process is the major reason for the enhanced oxidation capacity for electron-rich organic compounds (e.g., phenol) in the chloride-PMS system. However, we demonstrated that the chloride-PMS system clearly reduced the total organic carbon concentration (TOC), whereas the HOCl system did not lead to decrease in TOC. Overall, the chemical reaction is negligible in an aqueous condition if the concentrations of reagents are low, and freezing the solution accelerates the degradation of dye pollutants remarkably. Most notably, the pseudo-first order kinetic rate constant for acid orange 7 (AO7) degradation is approximately 0.252 h−1 with 0.5 mM PMS, 1 mM NaCl, initial pH 3, and a freezing temperature of −20 °C. AO7 degradation is not observed when the solution is not frozen. According to a confocal Raman-microscope analysis and an experiment that used an extremely high dose of reactants, the freeze concentration effect is the main reason for the acceleration phenomenon. Because the freezing phenomenon is spontaneous at high latitudes and at mid-latitudes in winter, and the chloride is ubiquitous elsewhere, the frozen chloride-PMS system has potential as a method for energy-free and eco-friendly technology for the degradation of organic pollutants in cold environments.

233 Inclusion of a multispecies fungal feed additive in forage-based diets fed to beef cattle: Effects on growth performance and ruminal fermentation

Abstract The objective was to evaluate the effect of adding a multispecies fungal feed additive (MFA; Aspergillus flavus, Aspergillus niger, Aspergillus oryzae) to forage-based diets fed to beef cattle on growth performance and ruminal fermentation. Experiment 1 evaluated the effect of supplementing Angus × SimAngus-crossbred steers [n = 80; initial body weight (BW) = 370 ± 44 kg] with varying doses of an MFA in a randomized complete block design. Steers were blocked by BW and housed in 8 feedlot pens (randomly assigned 2 pens per treatment) where a hay-based diet was fed for 122 d. The hay-based diet was offered with the inclusion of the MFA at 0.02, 0.04, and 0.08 % of the diet dry matter (DM), or without the inclusion of the MFA (CON). Steers were weighed at 28-d intervals. For experiment 2, ruminally cannulated Angus × SimAngus cows (n = 4; initial BW = 569 ± 21 kg) were used in a crossover design with two 21-d study periods to evaluate the effect of dietary inclusion of an MFA on in situ digestion and rumen metabolites. Treatments consisted of a forage-based diet with (WFA) or without (CON) the inclusion of the MFA. In situ digestion was evaluated on d 5, 10, and 20 throughout each period. In-situ bags were incubated in the rumen for 0 to 36 h, sampling every 4 h. On d 20, samples of ruminal fluid were collected to analyze short-chain fatty acids (SCFA) concentration. All data were analyzed using the PROC MIXED procedure of SAS. For experiment 1, a polynomial contrast was used. For experiment 2, the interaction between period and treatment was not significant (P &amp;gt; 0.45). In Experiment 1, the final BW, average daily gain (ADG), and gain to feed ratio (G:F) changed cubically (P ≤ 0.04; Table 1) as dietary inclusion of the MFA increased. Steers supplemented with the MFA at a rate of 0.02% of the diet DM were heavier at the end of the 122-d study period and had the greatest ADG and G:F among treatments. No differences between treatments (P ≥ 0.37) were observed for dry matter intake. In Experiment 2, no treatment × time interactions and treatment effects were detected (P ≥ 0.17; Table 2) for the in-situ disappearance rate and degradation kinetics of the diet DM, neutral detergent fiber, and acid detergent fiber. In addition, MFA supplementation did not affect (P ≥ 0.13; Table 3) the SCFA profile and the total SCFA content in the rumen fluid. Results from these studies indicate that dietary inclusion of an MFA might be an effective alternative to increase the feed efficiency of beef cattle-fed forage-based diets. However, the precise mode of action warrants further investigations.

Human Plasma Butyrylcholinesterase Hydrolyzes Atropine: Kinetic and Molecular Modeling Studies.

The participation of butyrylcholinesterase (BChE) in the degradation of atropine has been recurrently addressed for more than 70 years. However, no conclusive answer has been provided for the human enzyme so far. In the present work, a steady-state kinetic analysis performed by spectrophotometry showed that highly purified human plasma BChE tetramer slowly hydrolyzes atropine at pH 7.0 and 25 °C. The affinity of atropine for the enzyme is weak, and the observed kinetic rates versus the atropine concentration was of the first order: the maximum atropine concentration in essays was much less than Km. Thus, the bimolecular rate constant was found to be kcat/Km = 7.7 × 104 M-1 min-1. Rough estimates of catalytic parameters provided slow kcat < 40 min-1 and high Km = 0.3-3.3 mM. Then, using a specific organophosphoryl agent, echothiophate, the time-dependent irreversible inhibition profiles of BChE for hydrolysis of atropine and the standard substrate butyrylthiocholine (BTC) were investigated. This established that both substrates are hydrolyzed at the same site, i.e., S198, as for all substrates of this enzyme. Lastly, molecular docking provided evidence that both atropine isomers bind to the active center of BChE. However, free energy perturbations yielded by the Bennett Acceptance Ratio method suggest that the L-atropine isomer is the most reactive enantiomer. In conclusion, the results provided evidence that plasma BChE slowly hydrolyzes atropine but should have no significant role in its metabolism under current conditions of medical use and even under administration of the highest possible doses of this antimuscarinic drug.

Experimental study on the effect of circulating liquid velocity on bubble size distribution and turbulence characteristic in an external loop airlift reactor

AbstractThe influence of circulating liquid velocity on bubble size distribution (BSD) and turbulence characteristics of an external loop airlift reactor was studied in this paper. The instantaneous and time‐averaged velocity in the riser were studied using particle image velocimetry (PIV), and BSDs were measured by digital image analysis technique based on machine learning. Then turbulence kinetic energy (TKE) and energy dissipation rate (EDR) were calculated through the velocity field. The results indicate that as the circulating liquid velocity increased, the peak value of BSD rapidly decreased from nearly 6 mm to approximately 2 mm. The radial velocity of the liquid gradually decreased and changed direction, eventually increasing again. TKE first decreased and then increased. Compared with bubble flow with a BSD peak of 2–6 mm, bubble flow with a BSD peak of 2 mm had larger TKE. The radial movement of bubbles had great influence on the turbulence characteristics. This study demonstrates that selecting an appropriate circulating liquid velocity can reduce the diameter of bubbles while obtaining greater TKE, thereby improving the mass transfer and reaction efficiency in external loop airlift reactors (EL‐ALR).

A green and economic approach to synthesize magnetic Lagenaria siceraria biochar (γ-Fe2O3-LSB) for methylene blue removal from aqueous solution.

In the printing and textile industries, methylene blue (a cationic azo dye) is commonly used. MB is a well-known carcinogen, and another major issue is its high content in industrial discharge. There are numerous removal methodologies that have been employed to remove it from industrial discharge; however, these current modalities have one or more limitations. In this research, a novel magnetized biochar (γ-Fe2O3-LSB) was synthesized using Lagenaria siceraria peels which were further magnetized via the co-precipitation method. The synthesized γ-Fe2O3-LSB was characterized using FTIR, X-ray diffraction, Raman, SEM-EDX, BET, and vibrating sample magnetometry (VSM) for the analysis of magnetic properties. γ-Fe2O3-LSB showed a reversible type IV isotherm, which is a primary characteristic of mesoporous materials. γ-Fe2O3-LSB had a specific surface area (SBET = 135.30 m2/g) which is greater than that of LSB (SBET = 11.54 m2/g). γ-Fe2O3-LSB exhibits a saturation magnetization value (Ms) of 3.72emu/g which shows its superparamagnetic nature. The batch adsorption process was performed to analyze the adsorptive removal of MB dye using γ-Fe2O3-LSB. The adsorption efficiency of γ-Fe2O3-LSB for MB was analyzed by varying parameters like the initial concentration of adsorbate (MB), γ-Fe2O3-LSB dose, pH effect, contact time, and temperature. Adsorption isotherm, kinetic, and thermodynamics were also studied after optimizing the protocol. The non-linear Langmuir model fitted the best to explain the adsorption isotherm mechanism and resulting adsorption capacity ( =54.55mg/g). The thermodynamics study showed the spontaneous and endothermic nature, and pseudo-second-order rate kinetics was followed during the adsorption process. Regeneration study showed that γ-Fe2O3-LSB can be used up to four cycles. In laboratory setup, the cost of γ-Fe2O3-LSB synthesis comes out to be 162.75 INR/kg which is low as compared to commercially available adsorbents. The results obtained suggest that magnetic Lagenaria siceraria biochar, which is economical and efficient, can be used as a potential biochar material for industrial applications in the treatment of wastewater.

Enhanced Piezocatalytic Performance of Li-doped BaTiO3 Through a Facile Sonication-Assisted Precipitation Approach.

Piezocatalysis-induced dye degradation has garnered significant attention as an effective method for addressing wastewater treatment challenges. In our study, we employed a room-temperature sonochemical method to synthesize piezoelectric barium titanate nanoparticles (BaTiO3: BTO) with varying levels of Li doping. This approach not only streamlined the sample preparation process but also significantly reduced the overall time required for synthesis, making it a highly efficient and practical method. One of the key findingswas the exceptional performance of theLi-doped BTO nanoparticles. With 20 mg of Li additive, we achieved 90% removal of Rhodamine B (RhB) dye within a relatively short timeframe of 150 minutes, all while subjecting the sample to ultrasonic vibration. This rapid and efficient dye degradation was further evidenced by the calculated kinetic rate constant, which indicated seven times faster degradation rate compared to pure BTO. The enhanced piezoelectric performance observed in the Li-doped BTO nanoparticles can be attributed to the strategic substitution of Li atoms, which facilitated a more efficient transfer of charge charges at the interface. Overall, our study underscores the potential of piezocatalysis coupled with advanced materials like Li-doped BTO nanoparticles as a viable and promising solution for wastewater treatment, offering both efficiency and environmental sustainability.

Alkaline hydrolysis of poly (ethylene terephthalate) using 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU)

Advanced polymer recycling methods can address challenges with mechanical recycling caused by contaminated samples and mixed plastic wastes. In this work, we report alkaline hydrolysis of poly (ethylene terephthalate) (PET) flakes using a super basic reagent, 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU) in an aqueous media. The effect of operating conditions including temperature, time, and DBU concentration on the conversion of PET and the yield of terephthalic acid (TPA) was investigated. The relative hydrolysis kinetics were compared for the homogenous reaction of ethyl acetate and heterogenous PET reaction to elucidate the mechanism. While DBU exhibited much higher activity for both systems than NaOH at similar conditions, the increase in rate kinetics was much greater for the PET hydrolysis. This difference in kinetics was attributed to a combination of improved surface wetting of PET by DBU reaction media and the increased activity of the DBU. The hydrolysis of ethyl acetate was studied as a model system to determine the reactant's activity in a homogenous hydrolysis reaction. The effect of surface wetting was studied by conducting contact angle measurements of solutions.

Safety and effectiveness of portal vein embolization after hepatic arterial infusion therapy

Portal vein embolization (PVE) is a potential tool useful for inducing future liver remnant (FLR) hypertrophy in patients with advanced hepatic malignancies who are at high risk of hepatic insufficiency if treated by surgical resection. However, the safety and effectiveness of PVE in the context of patients who have undergone hepatic arterial infusion (HAI) is unknown. This retrospective, single-center study identified nine patients who underwent PVE after HAI between January 2015 and December 2022. There were no major adverse events, including biliary, or high-grade liver failure. Analysis showed an increase in standardized FLR from 21.1 ± 2.4% to 34.8 ± 2.1% over 9.8 ± 1.2 weeks, with a mean kinetic growth rate of 2.2 ± 0.6%. The study suggested compatibility of PVE after HAI. Patients who have undergone HAI therapy should not be excluded from consideration of PVE as part of their operative clearance strategy.

Reactive layered hydroxide membrane for advanced water treatment: Micropollutant degradation and antifouling potential

The effective removal of micropollutants by water treatment technologies remains a significant challenge. Herein, we develop a CoFe layered double hydroxide (CoFeLDH) catalytic membrane for peroxymonosulfate (PMS) activation to achieve efficient micropollutant removal with improved mass transfer rate and reaction kinetics. This study found that the CoFeLDH membrane/PMS system achieved an impressive above 98% degradation of the probe chemical ranitidine at 0.1 mM of PMS including five more micropollutants (Sulfamethoxazole, Ciprofloxacin, Carbamazepine, Acetaminophen and Bisphenol A) at satisfactory level (above 80%). Moreover, significant improvements in water flux and antifouling properties were observed, marking the membrane as a specific advancement in the removal of membrane fouling in water purification technology. The membrane demonstrated consistent degradation efficiency for several micropollutants and across a range of pH (4 to 9) as well as different anionic environments, thereby showing it suitability for scale-up application. The key role of reactive species such as SO4•–, and O2•− radicals in the degradation process was elucidated. This is followed by the confirmation of the occurrence of redox cycling between Co and Fe, and the presence of CoOH+ that promotes PMS activation. Over the ten cycles, the membrane could be operated with a flux recovery of up to 99.8% and maintained efficient performance over 24 h continuous operation. Finally, the efficiency in degrading micropollutants, coupled with reduced metal leaching, makes the CoFeLDH membrane as a promising technology for application in water treatment.