Ratio Of Chloride Research Articles

Modification of the Spin Transition Properties in hetero‐anionic Iron(II)‐triazole Complexes

The phenomenon which is called spin crossover is known to occur in some coordination compounds with an octahedral ligand field and electron configurations from 3d4 to 3d7. Thereby, a reversible transition between spin states (high spin and low spin state) is possible, through several external stimuli. Iron(II) triazole complexes exhibit this phenomenon at a wide range of temperatures depending on the ligands and anions used. For this reason, they are often considered for several possible practical applications. It is also possible to combine ligands or anions to modify the transition temperature. The latter of which was rarely discussed in the past. In this study we synthesized a series of iron(II)‐4‐Aminotriazole complexes, with different ratios of chloride‐ and tetrafluoroborate‐anions, of the formula [Fe(Atrz)3]Cl2‐X(BF4)X. We show that the combination of these anions leads to transition temperatures between those of their corresponding pure anion complexes. We furthermore present that a simple modification of the synthesis leads to a possible easy way of fine‐tuning transitions temperatures.

C-Reactive Protein-to-Serum Chloride Ratio: A Novel Marker of All-Cause Mortality in Maintenance Haemodialysis Patients

Background and Objectives: hypochloremia is an emerging risk factor for mortality in patients with chronic kidney disease. The pathophysiological mechanisms of this finding are not very clear. Some studies suggest the influence of inflammation as a synergistic factor, so we set out to analyse the association of a novel C-reactive protein-to-serum chloride ratio (CRP/Cl−) with the prognosis of maintenance haemodialysis patients and to assess its relationship with fluid status and body composition measured by bioimpedance. Materials and Methods: the present work is a retrospective cohort study of maintenance haemodialysis patients from our chronic outpatient haemodialysis programme between 1 January 2022 and 31 December 2022. (n = 281). Survival time was collected for all patients and analysed using the Kaplan–Meier method. A Cox proportional hazards regression model was used to evaluate survival probabilities. Variables included in the model were selected using a stepwise selection procedure based on the corrected Akaike information criterion (AICc), which balances model fit and complexity. Results: during a median follow-up of 306 days, 34 patients died. Patients in the fourth quartile of the CRP/Cl− (>0.118 mg/mEq) had higher overall mortality (log-rank test, p = 0.0011). In the Cox multivariate analysis, the variables significantly associated with higher mortality were higher modified Charlson index (MCI), lower body surface area (BSA), lower interdialytic weight gain (IDWG), and higher CRP/Cl− ratio. The latter variable was independently associated with higher overall mortality (adjusted hazard ratio = 1.027; 95% confidence interval [CI], 1.000–1.055 p = 0.0469). Conclusions: Higher CRP/Cl− ratio values were associated with higher all-cause mortality in our maintenance haemodialysis patients.

Performance of Cobalt-Doped C3N5 Electrocatalysis Nitrate in Ammonia Production

In this experiment, C3N5 was synthesized by pyrolysis of 3-amino-1,2,4 triazole material, and then 1% Co-C3N5, 3% Co-C3N5, 5% Co-C3N5, 7% Co-C3N5, and 9% Co-C3N5 were synthesized by varying the mass ratio of cobalt chloride to C3N5 by stirring and ultrasonic shaking. SEM, XPS, and XRD tests were performed on the synthesized materials. The experimental results showed that Co atoms were successfully doped into C3N5. The electrocatalytic reduction experiments were performed to evaluate their NH3 yields and electrochemical properties. The results showed that the ammonia yield obtained by the electrolysis of the 9% Co-C3N5 catalyst as the working electrode in a mixed electrolytic solution of 0.1 mol/L KNO3 and 0.1 mol/L KOH for 1 h at a potential of −1.0 V vs. RHE was 0.633 ± 0.02 mmol∙h−1∙mgcat−1, and the Faraday efficiency was 65.98 ± 2.14%; under the same experimental conditions, the ammonia production rate and Faraday efficiency of the C3N5 catalyst were 0.049 mmol∙h−1∙mgcat−1 and 16.41%, respectively, and the ammonia production rate of the C3N5 catalyst was nearly 13-fold worse than the 9% Co-C3N5, which suggests that Co can improve the Faraday efficiency and ammonia yield of the electrocatalytic reduction of NO3−. This is due to the strong synergistic effect between the cobalt and C3N5 components, with C3N5 providing abundant and homogeneous sites for nitrogen coordination and the Co-N species present in the material being highly efficient active sites. The slight change in current density after five trials of 9% Co-C3N5 and the decrease in ammonia yield by about 12% in five repetitions of the experiment indicate that 9% Co-C3N5 can be recycled and work stably in electrocatalytic reactions and has good application prospects.

Diffusion coefficients of Al<sub>2</sub>Cl<sub>7</sub><sup>–</sup> in low temperature chloroaluminate melt based on triethylamine hydrochloride

With the growing demand for renewable energy sources, much of the research in the battery industry is focused on creating safe and high-capacity energy storage systems that can handle high current loads using inexpensive and readily available materials. The aluminum-ion batteries (AIB) are considered as one of the most promising systems. Such materials as aluminum metal, carbon materials and chloroaluminate ionic liquids are used as anode, cathode and electrolyte, respectively. A low-temperature chloroaluminate melt based on triethylamine hydrochloride (Et3NHCl) is promising and inexpensive electrolytes for AIBs. This melt has the ability to reversibly precipitate/dissolve aluminum metal due to the presence of the Al2Cl7– ion in it. However, the diffusion of Al2Cl7– ions in the Et3NHCl–AlCl3 system has not been studied previously. In the presented work, the concentration dependence of the diffusion coefficients of the Al2Cl7– anion was studied using chronopotentiometry in the concentration range N = 1.3–1.95 (where N is the molar ratio of aluminum chloride to organic salt). It was shown that diffusion coefficients increase with aluminum chloride content growth in the studied melt: from 1.71·10–7 (N = 1.3) to 4.50·10–7 cm2·s–1 (N = 1.95). This behavior can be caused by the viscosity decrease of the melts with Al2Cl7– concentration growth. Based on the obtained results it can be concluded that Et3NHCl–AlCl3 with N = 1.95 is the most suitable electrolyte for AIB. Moreover, it was established that the electrochemical reduction of the Al2Cl7– on the surface of the aluminum electrode is complicated by the nucleation process, which has the lowest overvoltage at N = 1.95.

Sustainable fungi-based protein extraction from agro-waste mushroom stem using deep eutectic solvents

This study evaluated the nutritional and functional qualities of the mushroom stem (MS) powder and its protein concentrates, which were extracted using alkaline and deep eutectic solvent (DES)-based methods. MS powder is rich in protein (23.02 %) and carbohydrates (63.01 %). Alkaline extraction yielded the highest protein content (45.90 %) but lower recovery rates (15.39 %) compared to DES extractions using a 1:2 M ratio of choline chloride: glycerol (DES-CG) and choline chloride: lactic acid (DES-CL), which had recovery rates of 22.04 % and 21.47 %, respectively. DES solvents provided strong hydrogen bonding, as indicated by FTIR analysis, and produced uniform, smooth particles according to SEM imaging. Both DES and alkaline methods achieved similar protein solubility values (72–75 %). However, DES methods better preserved emulsion capabilities and balanced foaming properties, enhancing foam capacity and maintaining stability. The findings suggest that DES methods are more sustainable and efficient for extracting proteins from MS powder, optimizing both functional properties and environmental sustainability in food applications.

Impact of sulfate to chloride ratio on titanium aluminide coating's high temperature corrosion performance in settings mimicking waste incineration

One major problem with waste incineration is the corrosion of superheater tubes at high temperatures. The presence of sulfate and chloride in this setting poses a severe risk to the boiler's service life. In this work, pack aluminizing was used to create titanium aluminide coating, which was then subjected to five distinct NaCl+Na2SO4 salt combination proportions for 168 h at 600 °C. The outcomes demonstrated that in the presence of solid Na2SO4 deposits, titanium aluminide coating displayed remarkably low corrosion rates. Adding 1/6 NaCl significantly accelerated the rate of corrosion. The electrochemical corrosion resulting from eutectization between NaCl and Na2SO4 was again considerably amplified when the NaCl level was raised to 1/4.

Gel-type resin loaded with nano-hydrated ferric oxide for the removal of anions from papermaking wastewater

The main anions in papermaking wastewater are sulfate and chloride. In this paper, a strongly basic gel-type anion exchange resin (201×7) loaded with 20 ~ 200nm hydrated ferric oxide was prepared by dispersion impregnation with ethanol. The modified resin enhances the ability to remove sulfate by complexation of ligands to cause sulfate to form outer and inner sphere complexes on hydrated ferric oxide. The modified resin was dependent on acidic conditions, and the maximum exchange capacity for sulfate was enhanced by 14.2% under the optimal pH, exchange time, and ion concentration conditions. Competitive exchange experiments showed that the removal effect of the modified resin on chloride was almost unchanged under different chloride, sulfate ratios, and the degree of improvement of the removal effect on sulfate decreased from 9.5 ~ 5.5% with the increase of chloride ratio. The removal of sulfate by the modified resin was consistent with the proposed secondary kinetics and Langmuir adsorption model. In addition, the modified resin maintained 88% reuse after four desorption-adsorption cycles and achieved a regeneration rate of 93.1% after was eluted with HCl and reloaded with hydrated ferric oxide. The expected removal effect was well achieved when the resin was applied to the actual wastewater treatment. The above results indicate that the hydrated ferric oxide modification can improve the ability of the 201×7 resin to remove sulfate from water, and is a promising method for removing anions from papermaking wastewater.

Effects of Carbon-Based Modified Materials on Soil Water and Fertilizer Retention and Pollution Control in Rice Root Zone

To seek an appropriate stabilization and remediation scheme for cadmium (Cd) and arsenic (As) pollution in farmland, a typical polluted soil sample was selected from a mining area in Southwest China for a soil box simulation experiment. Biochar (BC), a modified type of biochar made from rice husk with different mass ratios of ferric chloride and rice husk, was set up (the mass ratio of ferric chloride to rice husk was 1:9 (defined as LFB), 3:7 (defined as MFB), and 5:5 (defined as HFB) and the control group (BL)) to explore the effects of soil water and fertilizer loss, the bioavailability of Cd and As, and the bioenrichment effects of plant organs during the growth period of rice. The results showed that the porous structure and large specific surface area of biochar effectively regulated soil aggregate composition and improved soil water holding capacity. Compared to the BL treatment, soil water storage under the four carbon-based material control modes increased from 8.98% to 14.52%. Biochar has a strong ion exchangeability and can absorb soil ammonium, nitrogen, and phosphoric acid groups, effectively inhibiting the loss of soil fertilizer. Biochar improves soil pH and reduces the specific gravity of exchangeable Cd. In addition, the oxygen-containing functional groups in biochar can react with metals in a complex manner. The diethylenetriaminepentaacetic acid (DTPA) concentrations of Cd in soils treated with BC, LFB, MFB, and HFB were 79.69%, 72.92%, 64.58%, and 69.27% lower, respectively, than those treated with BL. In contrast, the Fe3+ in ferric chloride combines with As after hydrolysis and oxidation to form amorphous ferric arsenate precipitates or insoluble secondary minerals. Therefore, the curing effect of the modified biochar on As was more potent than that of applied biochar alone. In conclusion, ferric chloride-modified biochar can effectively inhibit the effects of water and fertilizer loss in farmland soil and realize cross-medium long-term inhibition and control of combined Cd and As pollution.

NADES systems comprising choline chloride and polyphenols: Physicochemical characterization, antioxidant and antimicrobial activities

Natural Deep Eutectic Solvents (NADES) represent a new group of green and environmentally friendly solvents that comply with all the principles of green chemistry. NADES are formed via hydrogen bonding by combining hydrogen bond donors (HBD) and hydrogen bond acceptors (HBA). In this paper, we presented ten NADES systems based on choline chloride and different polyphenols. The basic physicochemical and biological properties were evaluated (stability, density, viscosity, FTIR, ORAC, antibacterial activity). It was shown that all the systems had a high densities and high dynamic viscosities. The densities ranged from 1.096 – 1.221 mg/mL for ChCl – resveratrol and ChCl – rutin, respectfully. The dynamic viscosities ranged from 0.247–1.662 Pa S for ChCl – gallic acid and ChCl – chlorogenic acid, respectfully. The viscosity could be lowered by increasing the molar ratio of choline chloride. Four NADES systems, comprising catechin, rosmarinic acid, gallic acid and chlorogenic acid could be diluted with water without affecting the stability of those systems. This finding could increase the usability of those systems. The FT-IR analysis of the selected systems showed that the peaks are widened and slightly shifted, without formation of new peaks, which proves the formation of hydrogen bonds between the NADES constituents. All tested systems showed high ORAC value (426.94–874.96 Trolox eq/mL) and antibacterial activity (0.625–2.5 % NADES).

Efficient continuous synthesis of long-chain alkylbenzenes catalyzed by ionic liquids in microreaction systems

Alkylbenzene (LAB) is an important benzene derivative that can be used as a raw material for high-performance anionic surfactants such as alkylbenzene sulfonates (LAS) to meet the new requirements for surfactants in many fields. LAB can be synthesized through Friedel-Crafts reaction in the presence of acidic catalysts as alkylating agents, which is commonly used in the production of fine chemicals. In this work, a novel and efficient continuous flow micro reaction system was introduced to enhance the production of long-chain alkylbenzene catalyzed by [(CH3)3NH][Al2Cl7] ionic liquid. The optimal conditions were investigated for the synthesis of long-chain alkylbenzenes with the 1-tetradecene and mixing α-alkenes of C14-C16 from Fischer-Tropsch process. The results showed that the yield of benzene alkylation can achieve 99 % under the optimal process conditions which the reaction tube length was 2000 mm, the reaction temperature was 30 ℃, the catalyst dosage was 0.30 mL/min and the molar ratio of aluminum chloride to trimethylamine hydrochloride was 2:1. In addition, α-alkenes with C14-C16 lead to deactivation of the ionic liquids catalyst easier because of transfer of AlCl3 from the ionic liquid to the organic phase compared to the pure 1-tetradecene as an alkylating agent. Continuous synthesis of the long-chain alkylbenzenes catalyzed by ionic liquids can achieve in the microchannel reaction system by controlling the flow patterns.

Efficient separation of cathode materials from aluminum foil by novel low-melting mixture solvent based on choline chloride-xylitol system

Lithium-ion batteries (LIBs) are important energy devices with significant growth and expansion that result in large amounts of metal waste. However, the separation of the cathode materials from aluminum (Al) foil during the recycling of spent LIBs is still challenging due to their strong bonding by polyvinylidene fluoride (PVDF). Herein, a novel low-melting mixture solvent (LoMMS) based on the choline chloride-xylitol system with ow-toxicity, cost-effectiveness, and environmental friendliness was developed for separating the cathode materials from Al foil in LIBs. Under the optimal treatment conditions of a molar ratio of choline chloride to xylitol of 2:1, a reaction temperature of 140 °C, a reaction time of 20 min, and solid-liquid ratio of 16 g/L separation efficiency cathode material reached a maximum of 94.92 %. The mechanistic analysis revealed that the high separation efficiency can be attributed to strong hydrogen bonding provided by choline chloride and xylitol in LoMMS, disrupted PVDF molecular bonding and resulted in deactivation and successful separation of cathode material particles from the aluminum foil. Additionally, scanning electron microscopy examination revealed no changes in the morphologies of the cathode materials, useful for their restoration and reutilization. Overall, the proposed LoMMS method with low-cost and eco-friendly aspects has great potential for recycling spent LIB cathode materials.

Magnetic carbon nanotube sorbents with macropores formed by salts for oily wastewater treatment

The development of carbon-based sorbents that are simple to fabricate, possess high sorption capacity and are easily collected and reusable has been of great interest for oily wastewater remediation. A magnetic carbon nanotube (CNT) oil sorbent is proposed to cleanup of oily wastewater, offering effortless and complete recovery and enabling reusability. The sorbent, characterized by easy preparation of multi-walled CNT (MWCNT) with m-cresol for macronization, is coupled with a space-holder technique that employs salts for open pore formation for oil sorption. Four sorbents were prepared with varying ratios of sodium chloride (NaCl) and monosodium L-glutamate (MSG), resulting in surface open pores corresponding to salt particle sizes. The sorbents formed an extensive macropore network of more than 200 μm while enhancing the specific surface area. Their bulk densities ranged from 126 kg/m3 to 139 kg/m3, indicating CNT powder densification and suitability for wastewater oil absorption. With its elongated rectangle shape, the MSG-prepared sorbent, exhibited the widest specific surface area and diverse macropores, including those larger than 800 μm. The sorbents exhibited sorption capacities of 2.37–13.60 g of oil/g of sorbent and volume gains of 44–123 %, depending on the oil and solvent types. These values were comparable to or exceeded those of previous carbon-based sorbents. The sorption capacities of the sorbents remained consistent over ten sorption-heat treatment cycles, highlighting recyclability. Sorbents of MWCNT grown from iron catalysts exhibited easy recovery by a magnet after oil sorption, with surface magnetism. Despite their promise for oily wastewater treatment, CNT sorbents must address challenges related to capacity improvement, scalability, economic viability, and environmental impact to be practical for widespread application.

Efficient recovery of gallium(Ⅲ) from alkaline solution by electrosorption using biomass-derived carbon aerogel electrodes

The effective extraction of gallium(Ⅲ) from alkaline solutions is a crucial strategy for the sustainable development of gallium resources. However, the conventional adsorption method is limited in terms of both the adsorption capacity and adsorption rate of gallium(Ⅲ). In this study, the optimal nitrogen-doped persimmon-powder activated carbon aerogel (NPAC) was prepared via optimizing synthesis conditions such as hydrothermal time, hydrothermal temperature, mass ratio of zinc chloride, and pyrolysis temperature to investigate the electrosorption effect of NPAC on gallium(Ⅲ). The results demonstrated that the electrode prepared from NPAC（NPAC@CF） exhibited exceptional electrochemical performance, attributed to the synergistic effect of reduced impedance, enhanced reversibility, and controlled capacitance (the capacitive contribution can be accurately quantified). At a bias voltage of 1.2 V, a pH of 11 and an initial concentration of NaGaO2 of 160 mg/L, the NPAC@CF electrode reached an outstanding electrosorption capacity of 250.69 mg g−1 for gallium(Ⅲ), which surpassed that of the conventional adsorption by over twofold. Electrosorption not only notably enhanced the adsorption capacity of NPAC for gallium(Ⅲ) but also elevated the adsorption rate, reducing the adsorption equilibrium time to just 40 min. The electrosorption mechanism of GaO2- on the surface of NPAC@CF was further understood by FTIR and XPS analyses, which mainly involved capacitive adsorption and the interaction of N/O-containing functional groups with GaO2-. Consequently, the electrosorption technology emerges as a promising, novel, and efficient approach for gallium extraction from alkaline solutions.

Thermodynamic properties of TPAC-EG deep eutectic solvents: A study based on the IGC method with molecular simulations

The study of thermodynamic properties and intermolecular interactions in deep eutectic solvents (DES) is an important innovative step in the development of DES. This research focuses on the synthesis of DES using a 1:2 M ratio of tetrapropylammonium chloride and ethylene glycol. Inverse gas chromatography (IGC) techniques are used to investigate DES of thermodynamics in the temperature range of 303.15–333.15 K. Additionally, molecular dynamics (MD) simulations and density functional theory (DFT) are used to explore intermolecular interactions in DES at both molecular and atomic levels. The research findings yield crucial insights, including the successful determination of infinite dilution activity coefficients, Flory-Huggin’s interaction parameters, solubility parameters, and Abraham solvation parameters of DES through IGC techniques. A careful study of the temperature-dependent trends in these parameters is provided. Analyses of structural properties, including radial distribution functions, hydrogen bond counts, and thermal fluctuation indices, reveal that, at experiments temperatures, the amount and nature of intermolecular hydrogen bonds in binary mixtures are the main factors influencing the thermodynamic properties of DES. Finally, based on DFT calculations, a quantitative assessment of the molecular interaction mechanisms of DES at the atomic level confirms the predominant role of hydrogen bonding in DES formation, with multicenter hydrogen bonds characterized by stronger hydrogen bond strengths emerging as the primary type.

#2967 C-reactive protein/serum chloride ratio: a novel marker of all-cause mortality in prevalent chronic haemodialysis patients

Abstract Background and Aims Serum chloride (Cl-) is an emerging marker of mortality in hypertension, sepsis, heart failure and chronic kidney disease. The pathophysiological mechanism is unclear, but haemodynamic and inflammatory factors have been suggested. As C-reactive protein (CRP) is an established marker of inflammation and prognosis in haemodialysis patients, we sought to determine whether there is an association between the CRP/Cl- ratio and prognosis in these patients. Method Retrospective cohort study. We included n = 281 prevalent patients in our chronic haemodialysis programme between 19 January 2022 and 11 August 2022. The mean follow-up was 10 months. The sample was divided into quartiles according to CPR/Cl— ratio values. Baseline demographic, analytical and bioimpedance data were collected (Table 1). Survival time was recorded in all patients and analysed using the Kaplan-Meier method. Results The median CPR/Cl— ratio was 0.04 mg/mEq (0.02; 0.12). Women accounted for 31.8%. 28.9% had underlying diabetic nephropathy. Overall survival at 10 months was 87.9%. Patients who died had a higher CPR/Cl— value [0.12 (0.04; 0.19)] vs [0.04 (0.02; 0.10)] (p = 0.0005). In addition, those in the fourth quartile had a lower probability of survival compared to the other quartiles (p = 0.0011, log-rank test) (Fig. 1). Conclusion Higher values of the CPR/Cl index were associated with higher all-cause mortality in our sample of prevalent haemodialysis patients.

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

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 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 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 min 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.

Synergistic effect of seaweed extract and boric acid and/or calcium chloride on productivity and physico-chemical properties of Valencia orange.

Many citrus species and cultivars are grown successfully in tropical and subtropical countries, as well as in arid and semi-arid regions with low levels of organic matter and low cation exchange, resulting in lower nutrient uptake by the plant. The essential nutrients needed for citrus flowering and fruit set are limited in winter due to a reduction in transpiration rate, negatively effecting vegetative growth, flowering, yield, and fruit quality. The present investigation was carried out to assess the nutritional status, fruit yield parameters, and fruit quality of Valencia orange trees after foliar spraying of seaweed extract (SW) combined with calcium chloride and boric acid and their combinations in the 2020/2021 and 2021/2022 seasons. The treatments were arranged in a split-plot design (three levels spraying seaweed extract × four levels spraying calcium chloride and boric acid and their combinations × four replicates × one tree/replicate). The results indicated that all of the characteristics measured, including leaf chlorophyll, leaf mineral contents, fruit yield parameters, fruit physical properties, and fruit chemical properties, were significantly affected by the foliar spraying of seaweed extract (SW) combined with calcium chloride and boric acid and their combinations. Although all treatments increased the productivity and the physical and chemical properties of Valencia orange fruits compared to the control, a treatment of 10 g/L SW combined with 0.5 g/L boric acid and 1 g/L calcium chloride produced superior results. This ratio of SW, boric acid, and calcium chloride is therefore recommended to enhance productivity and improve the physico-chemical properties of Valencia orange for greater fruit yield.

Investigation of oligomeric proanthocyanidins extracted from Rhodiolae Crenulatae Radix et Rhizomes using deep eutectic solvents and identified via data-dependent-acquisition mass-spectroscopy

In this study, 34 deep eutectic solvents were successfully prepared for the extraction of proanthocyanidin from Rhodiolae Crenulatae Radix et Rhizomes. The extraction process was optimized using single factor exploration and Box-Behnken design-response surface analysis. The extraction rate was significantly improved when the molar ratio of choline chloride to 1,3-propanediol was 1:3.5 and the water content was 30% (V/V) in deep eutectic solvents. AB-8 macroporous resin and ethyl acetate were used for separation and refining, and the oligomer-rich proanthocyanidin components were eventually obtained. The ultraviolet (UV) and infrared spectrometer (IR) spectra showed that the proanthocyanidins were mainly composed of catechin and epicatechin. To further clarify the chemical composition of proanthocyanidin, an ion scan list containing 156 proanthocyanidins precursors was obtained by constructing a proanthocyanidins structural library and mass defect filtering algorithm, combined with the Full mass spectrometry (MS)/dd-MS2 scan mode that turns on the “if idle pick others” function. By using Ultra high performance liquid chromatography & High-resolution mass spectrometer (UHPLC/Orbitrap MS), the analysis used both targeted and non-targeted methods to detect proanthocyanidins. Finally, 50 oligomeric proanthocyanidin compounds were identified, including 7 monomers, 22 dimers, 20 trimers, and 1 tetramer, most of which were procyanidins of proanthocyanidins (84%), and a small amount of prodelphinidin (14%) and other types of proanthocyanidins (2%), which enabled the systematic characterization of proanthocyanidin components from Rhodiolae Crenulatae Radix et Rhizomes. Meanwhile, the comparison with the grape seeds oligomeric proanthocyanidins standard (United States Pharmacopoeia) revealed that the proanthocyanidins in Rhodiolae Crenulatae Radix et Rhizomes were more abundant, suggesting that the proanthocyanidins in Rhodiolae Crenulatae Radix et Rhizomes has promising applications.

Preparation and study of the effect of pH value on structural, morphological, electrical and magnetic properties of CoFe2O4 nanoparticles prepared by sol-gel precipitation method

The present study reports the synthesis of cobalt ferrite nanoparticles (CoFe2O4 NPs) using the sol-gel precipitation process via mixing a stoichiometric ratio of cobalt chloride (1 M) and ferric chloride (2 M). The molar of ferric to cobalt was mentioned (2:1) and then 2 M of sodium hydroxide was added. The structural and morphological features of the material were assessed using X-ray diffraction (XRD), Scanning electron microscopy (SEM), and atomic force microscopy (AFM). The electrical properties were analyzed using an LCR meter, while the magnetic properties were measured using a vibrating sample magnetometer (VSM). Fourier-transform infrared spectroscopy (FTIR) investigated the material's molecular vibrations. The X-ray diffraction (XRD) analysis revealed that all the samples exhibited a cubic spinal structure, and no additional peak was detected. Interestingly, the average size of the crystallites (D) decreased from 17.74 nm to 16.58 nm as the pH level increased from 7 to 13. This finding provides important insights into the behaviour of the tested samples under different pH conditions. The formation of the ferrite spine was confirmed by FTIR spectroscopy, with the primary detected bands (408.92–470.65 cm−1) attributed to the octahedral complexes and (516.94–588.31 cm−1) assigned to the tetrahedral ones. The dielectric and imaginary part of the dielectric constant decreased with increasing pH values excluding samples prepared at pH = 11. All samples with different pH values exhibit resonance peaks at frequencies up to (1 KHz). The magnetic measurements carried out by the VSM instrument, the result show that the saturation magnetization increases with increasing pH and the higher saturation magnetization is 68 emu. g1.

Innovative deep decontamination of radioactive solid surfaces using microemulsions of deep eutectic solvents in supercritical carbon dioxide

Radioactive solid wastes resulting from the application of nuclear energy pose a risk to the environment, yet traditional decontamination methods generate many secondary wastes. Thus, sustainability-driven innovations are receiving increasing attention to achieve eco-friendly decontamination methods characterized by minimizing secondary waste generation. Here, we proposed a sustainable and pioneering approach to decontaminate radioactive solid wastes using microemulsions of deep eutectic solvents (DESs) in supercritical carbon dioxide (SC-CO2). We also determined the optimal ratios of the additives as follows: prepared DESs with a molar ratio of choline chloride (ChCl) to p-toluenesulfonic acid monohydrate (ptsa) of 1:2, and nonyl phenol polyoxyethylene ether (NP-10) to ChCl:ptsa DESs in a molar ratio of 0.8. Remarkably, after optimization of the decontamination process in terms of pressure, temperature and cleaning time, the radioactivity on the sample surface can be reduced to a level that is reusable in the nuclear field. Detailed analyses provided insights into the intermolecular interactions within the DESs. And the decontamination mechanisms involved the spontaneous evolution of microemulsions with ChCl:ptsa as the core to facilitate the solvation and removal of radioactive contaminants. Additionally, repeated cleaning was proved to be effective for ultra-deep decontamination, with the radioactivity on the sample surface reaching a clearance level and a decontamination efficiency of 99.8%. The DESs-in-CO2 systems successfully decontaminated various materials and simulated radionuclides, even real radioactive metal wastes from the nuclear industry. It was notable that the DESs-in-CO2 systems achieved decontamination efficiencies of more than 95.0% for radioactive contaminants on these solid surfaces. Overall, this innovative approach provided a green alternative to conventional radioactive solids decontamination, meeting the need for sustainable development of nuclear energy.