Sulfonic Acid Research Articles

Effects of perfluoroalkyl sulfonic acids on developmental, physiological, and immunological measures in northern leopard frog tadpoles

The chronic toxicity of short chain perfluoroalkyl sulfonic acids (PFSAs), such as perfluorobutanesulfonic acid (PFBS) and perfluorohexanesulfonic acid (PFHxS), are relatively understudied despite the increasing detection of these compounds in the environment. We investigated the chronic toxicity and bioconcentration of PFBS and PFHxS using northern leopard frog (Rana [Lithobates] pipiens) tadpoles. We exposed Gosner stage (GS) 25 tadpoles to either PFBS or PFHxS at nominal concentrations of 0.1, 1, 10, 100, and 1000 μg/L until metamorphosis (GS42). We then assessed tadpole growth, development, stress, and immune metrics, and measured fatty acid (FA) composition and PFSA concentrations in liver and whole-body tissues. Tadpole growth and development measures were relatively unaffected by PFSA exposure. However, tadpoles exposed to 1000 μg/L PFBS or PFHxS had significantly increased hepatosomatic indexes (HSI) relative to controls. Further, tadpoles from the 1000 μg/L PFHxS treatment had altered FA profiles relative to controls, with increased total FAs, saturated FAs, monounsaturated FAs, and omega-6 polyunsaturated FAs. In addition, tadpoles from the 1000 μg/L PFHxS treatment had a higher probability of waterborne corticosterone detection. These results suggest that PFBS and PFHxS influence the hepatic health of tadpoles, and that PFHxS may alter lipid metabolism in tadpoles. We also observed a higher probability of tadpoles being phenotypically female after exposure to an environmentally relevant concentration (0.1 μg/L) of PFHxS, suggesting that PFHxS may exert endocrine disrupting effects on tadpoles during early development. The measured bioconcentration factors (BCFs) for both compounds were ≤10 L kg−1 wet weight, suggesting low bioconcentration potential for PFBS and PFHxS in tadpoles. Many of the significant effects observed in this study occurred at concentrations several orders of magnitude above those measured in the environment; however, our work shows effects of PFSAs exposure on amphibians and provides essential information for ecological risk assessments of these compounds.

Secondary utilization of self-suspending proppant's coating polymer: Enhance oil recovery

Fracturing is associated with significant economic costs, and the loss of the utility of the self-suspending proppants' coating polymer after fracturing appears highly wasteful. To enhance the utilization of the self-suspending proppant's coating polymer, we propose a novel concept: the secondary utilization of coating polymer, enabling the coating polymer to gel-breaking within the reservoir and generate surface-active substances, thereby enhancing the oil recovery efficiency. To realize this concept, this study designed and synthesized a hydrophobic associative polymer, which was combined with ceramic proppant to form self-suspending proppant. Using the surface-active monomer octadecyl dimethyl allyl ammonium chloride (DMDAAC-18), acrylamide (AM), acrylic acid (AA), and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) via aqueous free-radical copolymerization synthesized the PAAAD (Polymer (AM/AA/AMPS/DMDAAC-18)). PAAAD has demonstrated excellent thickening properties, with a viscosity of 240.01 mPa s at a concentration of 6 g/L in shear rate 170s−1. Its solution exhibits high viscoelasticity, and a loss factor (tan δ) < 1 over the frequency range of 0–20 Hz at a shear stress of 0.56 Pa indicates that it behaves like a viscoelastic solid with gel-like characteristics, which is beneficial for proppant suspension. The gel-breaking solution of PAAAD reduced surface tension (29.33 mN/m at a PAAAD concentration of 6 g/L), converted oil-wet rocks to water-wet conditions (reducing the contact angle of oil-wet shale to 46.7° and of oil-wet sandstone to 19.9°), and enhanced shale imbibition oil recovery efficiency in 16.5%. The basic properties of self-suspending proppants meet the Chinese Petroleum Industry Standard SY/T 5108-2014 and exhibit good suspension properties, with sedimentation of 1.7 mm in 40 min at a sand ratio of 15%. This study is the first to propose the secondary utilization of the self-suspending proppant's coating polymer, significantly enhancing their utilization value.

Enhanced Vanadium Redox Flow Battery Performance with New Amphoteric Ion Exchange Membranes.

Vanadium redox flow batteries (VRFBs) depend on the separator membrane for their efficiency and cycle life. Herein, two amphoteric ion exchange membranes are synthesized, based on sulfonic acid group-grafted poly(p-terphenyl piperidinium), for VRFBs. Using ether-free poly(p-terphenyl piperidine) (PTP) as the polymer matrix, and sodium 2-bromoethanesulphonate (ES) and 1,4-butane sultone (BS) as grafting agents, We achieve quaternization of PTP through an environmentally friendly process without alkaline catalysts. PTP-ES and PTP-BS membranes exhibit low area resistance, high H+ permeability, and significantly reduced vanadium ion permeability, leading to exceptional ion selectivity, which is 3.06×106Smincm-3 and 4.34×106Smincm-3, respectively,three orders of magnitude higher than that of Nafion115 (0.27×104Smincm-3). The VRFB with PTP-BS achieves a self-discharge duration of 190h, compared to 86h for Nafion 115. Additionally, under current densities of 40-160mAcm-2, PTP-BS shows coulombic efficiencies of 98.1-99.1% and energy efficiencies of 92.0-82.1%, outperforming Nafion 115. The VRFB with PTP-BS also demonstrates excellent cycle stability and discharge capacity retention over 300 cycles at 100mAcm-2. Therefore, the amphoteric PTP-BS membrane shows remarkable performance, offering significant potential for VRFB applications.

The Efficient Separation of Apatite from Dolomite Using Fucoidan as an Eco-Friendly Depressant

The aim is to explore new depressants for achieving the efficient separation of apatite and dolomite. In this work, fucoidan (FD) was examined as an eco-friendly dolomite depressant to separate dolomite from apatite. The depression ability and adsorption mechanisms were investigated. The flotation results indicated that FD selectively depressed dolomite. The flotation difference between dolomite and apatite reached 70% approximately at an FD concentration of 75 mg/L. Meanwhile, the recovery and grade of P2O5 reached 89.84% and 32.88% and that of MgO decreased to 1.64% and 34.24% in the artificially mixed minerals test. Wettability, zeta potential, and Fourier transform infrared spectroscopy (FTIR) results revealed that FD tended to adsorb onto dolomite, impeding the interaction of sodium oleate (NaOL) with dolomite, but barely affected that on apatite. Microcalorimetry analysis indicated that the adsorption heat of FD on dolomite was much higher and less time was required to achieve equilibrium. X-ray photoelectron spectroscopy (XPS) results proved that the sulfonic acid radicals within FD chemically interacted with Mg atoms on dolomite while it weakly adsorbed on apatite.

Phosphomolybdic acid functionalized nano silica for enhanced anti-biofouling effect in polymer electrolyte membranes for microbial fuel cell application

Microbial fuel cells (MFCs) represent a promising technology for simultaneous electricity generation and wastewater treatment. In this study, a single-chambered MFC was fabricated utilizing a novel polymer electrolyte membrane synthesized from sulfonated polyether ether ketone grafted with styrene sulfonic acid (SPEEK/SSA) as the base polymer, and silica decorated with phosphomolybdic acid (SPMA) as a functionalized nanofiller. Various concentrations of SPMA (2.5 %, 5 %, 7.5 %, and 10 %) were incorporated into the SPEEK/SSA membranes and characterized physicochemically. The SPEEK/SSA membrane with 5 wt% SPMA demonstrated the highest proton conductivity (3.75×10−2 S cm−1) and ion exchange capacity (1.68 meq g−1). This PEM also exhibited superior tensile strength (20 MPa) and excellent chemical durability, as evidenced by Fenton's reagent test. Performance evaluation revealed that this membrane achieved a maximum power density of 196.6 mW m−2 at a maximum of 180 mA m−2 current density. Additionally, antibiofouling tests indicated that the 5 % SPMA-incorporated membrane possessed significant antibacterial properties against both gram-positive and gram-negative bacteria and exhibited high biofilm inhibition. The wastewater treatment efficacy of the MFC with the 5 % SPMA membrane was confirmed by a chemical oxygen demand (COD) removal efficiency of 81.49 %, indicating its potential for effective wastewater treatment. Phylogenetic analysis through 16S rRNA sequencing identified major bacterial phyla including Proteobacteria, Bacteroidetes, Chloroflexi, and Firmicutes, with predominant genera such as Pseudomonas and Acidovorax. This study emphasises the potential of nanocomposite membranes to enhance the performance and durability of MFCs while mitigating biofouling, thereby paving the way for future research and development in this field.

Anoxic Manganese Bioleaching – Investigation of Scale-up Parameters in a Stirred Bioreactor

Presently huge operation costs arising from aeration and high electron donor requirements accompanied by low metal recovery rates are some impediments to the large-scale application of bioleaching for low-grade ores. The current study investigates key parameters for scaling up anoxic bioleaching, which overcomes some of the above shortcomings, on polymetallic manganese nodules using soil-based manganese-reducing bacterial consortia in a stirred bioreactor. Operating conditions such as carbon source concentration and pulp density were optimized. Parameters like pH, oxidation–reduction potential (ORP), and microbial growth were monitored in the bioreactor in both stirred and non-stirred conditions. The Mn(IV) reduction and dissolution in the bioreactor was 27 (±2.8)% over 30 days, which significantly enhanced to 43 (±1.5)% and 42 (±0.35)% in the presence of humic acid and anthraquinone sulfonic acid, respectively, in 15 days. A maximum dissolution of 21 (±4.1)% Cu, 10 (±3.0)% Ni, 18 (±4.7)% Co and 7 (±3.9)% Fe were also obtained with 100 µM humic acid from the agitated bioreactor in 15 days. The corresponding specific glucose consumption rate per unit mass of ore was found to be 27 mg g−1 day−1, which is 10 times lower than the rates reported previously for aerobic bioleaching methods. The investigation shows that mild agitation can significantly improve the anoxic bioleaching, especially with added electron shuttles, to enable better ore-bacteria interaction and prevent ore compaction during scale-up. The pH and ORP of the system point toward a reductive dissolution of Mn by the organisms.

Unique Core-Shell Structured Polyaniline Nanofibers Toward Ultrahigh-Rate Flexible All-Solid-State Supercapacitor.

Promoting charge storage and fast charging capability simultaneously is a long-standing challenge for supercapacitors. A facile flowing seed polymerization is adopted to prepare polyaniline (PANI) nanofibers, in which phytic acid (PA) doped oligomers are first produced as the seeds for promoting the highly oriented growth of PANI nanofibers accompanying with the copolymerization of m-aminobenzene sulfonic acid (ASA) and aniline occurred on the surface of PANI nanofibers, as a result, unique core-shell structured PANI nanofibers are continuously fabricated. Benefitting from compact nanofiber structure, excellent dispersion, and self-doping effect, as-prepared PANI nanofibers exhibit a specific capacitance of 671.2 F g-1 at 2 A g-1 and ultrahigh rate capability of 93.1% from 2 to 100 A g-1. Then assembled all-solid-state supercapacitor can deliver the highest energy density of 28.3Wh kg-1 at a power density of 320.2W kg-1 with remarkable rate capability (81.2% from 1 to 20 A g-1), cycle stability (77.5% after 5000 cycles) as well as light weight and flexibility. It is highly desirable that the present green and scalable approach can be further applied to fabricate other unique core-shell structured PANI nanofibers with appealing potentials in energy storage devices.

Synthesis and Dye Adsorption Dynamics of Chitosan-Polyvinylpolypyrrolidone (PVPP) Composite.

One major environmental issue responsible for water pollution is the presence of dyes in the aquatic environment as a result of human activity, particularly the textile industry. Chitosan-Polyvinylpolypyrrolidone (PVPP) polymer composite beads were synthesized and explored for the adsorption of dyes (Bismarck brown (BB), orange G (OG), brilliant blue G (BBG), and indigo carmine (IC)) from dye solution. The CS-PVPP beads demonstrated high removal efficiency of BB (87%), OG (58%), BBG (42%), and IC (49%). The beads demonstrated a reasonable surface area of 2.203 m2/g and were negatively charged in the applicable operating pH ranges. TGA analysis showed that the polymer composite can withstand decomposition up to 400 °C, proving high stability in harsh conditions. FTIR analysis highlighted the presence of N-H amine, O-H alcohol, and S=O sulfo groups responsible for electrostatic interaction and hydrogen bonding with the dye molecules. A shift in the FTIR bands was observed on N-H and C-N stretching for the beads after dye adsorption, implying that adsorption was facilitated by hydrogen bonding and Van der Waals forces of attraction between the hydroxyl, amine, and carbonyl groups on the surface of the beads and the dye molecules. An increase in pH increased the adsorption capacity of the beads for BB while decreasing OG, BBG, and IC due to their cationic and anionic nature, respectively. While an increase in temperature did not affect the adsorption capacity of OG and BBG, it significantly improved the removal of BB and IC from the dye solution and the adsorption was thermodynamically favoured, as demonstrated by the negative Gibbs free energy at all temperatures. Adsorption of dye mixtures followed the characteristic adsorption nature of the individual dyes. The beads show great potential for applications in the treatment of dye wastewater.

Short-side-chain perfluorinated polymeric membranes annealed at high temperature: Structure, conductivity, and fuel cell performance

The relationship between the mechanical, electrical, and morphological properties of annealed films based on short-side-chain perfluorinated sulfonic acid ionomer (SSCI) with an Aquivion structure was systematically investigated using dynamic mechanical analysis (DMA), small-angle X-ray scattering (SAXS), and impedance spectroscopy. Annealing the membranes at temperatures of 140, 150, and 160 °C—above the glass transition temperature of SSCI—and the nature of the liquid phase in the polymer dispersion significantly influence the structural parameters of the membranes, specifically the size of the conductive channels formed by hydrophilic sulfonic acid groups. SAXS and AFM analyses revealed that membranes cast from N,N-dimethylacetamide (DMAA) exhibit a denser, less structured morphology, resulting in lower hydrogen permeability (φ = 4.6 ± 0.7 nmol/m/s/MPa), comparable to the commercial Nafion 211 membrane (φ = 6.5 nmol/m/s/MPa), but with significantly lower proton conductivity (35 ± 5 mS/cm) than Nafion 211 (95 mS/cm). In contrast, membranes obtained from a water-alcohol mixture showed a well-defined structure (SAXS, AFM), with proton conductivity values ranging from 70 to 103 mS/cm, comparable to Nafion 211. However, the hydrogen permeability of these membranes varied significantly depending on the annealing conditions (φ = 5.5–65.3 nmol/m/s/MPa). SAXS data indicated that the membranes had a similar degree of crystallinity (11–13%) but differed in the positions of the ionomer peak and matrix knee, which are associated with variations in the size of the conductive channels and account for the observed differences in ionic conductivity. Membranes annealed at 150 °C, which exhibited hydrogen permeability and ionic conductivity values close to those of the commercial Nafion 211 membrane, were used to fabricate membrane electrode assemblies (MEA). The electrochemical characteristics of these MEAs were investigated at 30 and 60 °C, 100% relative humidity, at both atmospheric pressure and 200 kPa overpressure. At a current density of 1.75 A/cm2, the fabricated membranes demonstrated power outputs of up to 550 and 950 mW/cm2, which are comparable to, and even exceed, those of the commercial Nafion 211 membrane (700 mW/cm2). However, despite the high-power performance, significant membrane degradation was observed after 10,000 cycles in durability tests. These findings contribute to a better understanding of the relationship between the electrochemical properties and the structure of short-side-chain perfluorinated sulfonic acid ionomers with an Aquivion-type structure and are expected to enhance their application in fuel cells.

Orientation Control of Perfluorosulfonic Acid Films via Addition of 1,2,4-Triazole during Casting.

Perfluorosulfonic acid (PFSA) polymers are used as electrolyte membranes in polymer electrolyte fuel cells. To investigate the effect on proton conductivity through structural orientation control, we added 1,2,4-triazole to PFSA films during casting to impart anisotropy to the ion-cluster structure of the films. The proton conductivities of the films were found to be high in the film-surface direction and low in the film-thickness direction. Structural analysis using small-angle X-ray scattering suggested that the anisotropy in proton conductivity was due to anisotropy in the ion-cluster structure, which in turn was attributed to the formation of a phase-separated structure via strong bonding between sulfonic acid groups and 1,2,4-triazole during cast film formation and the surface segregation of fluorine. We expect the findings of this study to aid in the fabrication of PFSA films with controlled ion clusters.

Perfluorodecanoic acid induces the increase of innate cells in zebrafish embryos by upregulating oxidative stress levels

Several studies reported that the widespread use of perfluoroalkyl and polyfluoroalkyl substances (PFASs) causes increased environmental pollution, subsequently impacting aquatic organisms. Perfluoroalkyl substances such as perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) reportedly cause cardiotoxicity, neurotoxicity, and developmental toxicity in different organisms. However, whether perfluorodecanoic acid (PFDA), a widely used perfluoroalkyl substance, induces animal embryos developmental toxicity remain unknown. Here, we explored the immunotoxicity and associated mechanisms of PFDA in zebrafish embryos via RNA sequencing, morphological assessment and behavioral alteration detection following exposure to 0.5, 1 and 2 mg/L of PFDA. Interestingly, We found that with the increase of PFDA to drug concentration, including neutrophils and macrophages, significantly increased the number of inherent cells, immune related genes expression. Furthermore, oxidative stress increased in the PFDA-treated embryos in a dose-dependent manner and inhibition of oxidative stress levels effectively rescued the number of neutrophils. Changes in embryonic behavior were observed after exposure to PFDA. Overall, our results suggest that PFDA may induce innate immune response by accumulation of oxidative stress in zebrafish at early developmental stages, and concern is needed about its environmental exposure risks for animals embryos development. Environmental implicationPerfluorinated and polyfluorinated alkyl substances (PFASs) are a class of synthetic organic compounds containing fluorine widely used as lubricants, surfactants, insecticides, etc. The PFDA, a typical perfluorinated compound, is often used as a wetting agent and flame retardant in industries.Several studies showed that PFASs can cause serious environmental pollution, leading to developmental toxicity to various animals, including reproductive toxicity, liver toxicity, heart toxicity, neurotoxicity, and immunotoxicity.However, there are still limited studies on the effects and mechanisms of PFDA on aquatic organisms. Therefore, there is a need to evaluate the ecological risks of PFDA in animals.

Association between family economic situation and serum PFAS concentration in American adults with hypertension and hyperlipemia

Although there is an association between income status and concentration of perfluoroalkyl and polyfluoroalkyl substance (PFAS), the association remains uncertain in patients with hypertension, hyperlipidemia, and comorbidities. Data from the 2013–2016 National Health and Nutrition Examination Survey were analyzed. A total of 2665 adults were included, and the data included participants' serum PFAS (perfluorooctanoic acid [PFOA], perfluorononaic acid, perfluorodecanoic acid, perfluoroundecanoic acid, perfluorohexane sulfonic acid, and perfluorooctane sulfonic acid) levels and selected covariates. Multivariate linear regression models were used to examine the association between the ratio of family income to poverty (PIR) and individual serum PFAS concentrations in the hypertensive and/or hyperlipidemia groups after adjusting for covariates. The potential effects of sex and age on the results were explored using stratified analysis. A mediating effect model was used to explore the mediating effects of body mass index (BMI) and waist circumference on the association results. After adjusting for potential confounders, for hyperlipidemia and comorbidities (hypertension and hyperlipidemia), serum levels of multiple common PFAS increased by 0.09% (95%Confidence interval [CI] 0.02–0.15%) to 0.13% (95%CI 0.08–0.19%) and 0.10% (95%CI 0.02–0.17%) to 0.12% (95%CI 0.06–0.18%), respectively, with each 1% increase in PIR. The covariate model and stratified analyses results suggested the potential effects of different covariates such as age and sex, leading to changes in the statistical significance of the association results. BMI significantly mediated the effect of PIR on PFOA in hyperlipidemia (13%, P < 0.001). Household income in adults with hyperlipidemia and comorbidities positively correlated with serum PFAS concentration in the United States. Obesity played an indispensable mediating role in the association between economic income and PFAS concentration.

Synthesis and Characterization of Fe3O4@SiO2@APIDSO3H as a Novel and Efficient Magnetic Nanocatalyst in Pechmann Condensation

ABSTRACTFe3O4@APIDSO3H as a novel and magical magnetic nanocatalyst was designed, synthesized, and characterized by different spectroscopic techniques such as Fourier transform infrared (FT‐IR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), x‐ray diffraction (XRD), energy‐dispersive x‐ray (EDX), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The loading percentage of sulfonic acid on the magnetic nano catalyst was calculated using CHNS analysis. Then, the potential use of it was investigated for the synthesis of various coumarins by Pechmann condensation. The corresponding products were synthesized and isolated in 60%–99% yields. The catalyst was recycled and reused for four times without loss in catalytic activity.

Efficient cascade reactions involving esterification, hydrogen transfer, and lactonization for biomass conversion using MOF/Metal oxide composites as heterogeneous catalysts

Development of heterogeneous catalysts with both Brønsted and Lewis acid properties has proved to be promising and useful because they offer an efficient way to cascade reactions. In this study, we present the synthesis pathway and efficacy evaluation of new composites which combined by sulfonic acid functional group modified TiO2 and MIL-101, analyzing their structure-performance correlation as heterogeneous catalysts in cascade reactions involving esterification, hydrogen transfer, and lactonization. These composites possess an open porous structure (MOF and porous TiO2), as well as active sites including Lewis acid (unsaturated coordination metal), Lewis base (Ti-OH), and Brønsted acid (-SO3H). The role of these active sites and the synergies between them were investigated through the esterification of levulinic acid and the direct synthesis of γ-valerolactone from levulinic acid and furfural under cascade reactions. The composites exhibit a 100% ethyl levulinate (EL) yield at 120°C for 6 hours, with γ-valerolactone yields reaching up to 94.5% (160 °C, 9 h) and 89.5% (160 °C, 16 h) from levulinic acid and furfural, respectively. This synergistic effect of Lewis acid/base and Brønsted acid ensures efficient esterification. The presence of a sulfonic acid group promotes the lactonization reaction, while the Meerwein-Ponndorf-Verley reduction is facilitated by the dual Cr sites located adjacent to each other in the secondary building unit of MIL-101(Cr). Moreover, the double-porous structure of porous TiO2 and MIL-101(Cr) effectively guarantees the efficient mass transfer of reactants and intermediates, leading to enhanced synergistic effects that promote more efficient reaction conversion.

Exploring methandienone metabolites generated via homogenized camel liver: Advancements for anti-doping applications through High Resolution-Liquid Chromatography Mass Spectrometry analysis.

Anabolic steroids, also known as anabolic-androgenic steroids (AAS), encompass steroidal androgens such as testosterone, as well as synthetic counterparts with similar structures and effects. The misuse of AAS has increased over the years, leading to ethical and welfare concerns in sports. The World Anti-Doping Agency (WADA) and the International Federation for Equestrian Sports (FEI) have banned AAS in relevant sports. Methandienone is one of the most identified anabolic androgenic steroids in sports drug testing, Therefore, reliable detection methods are crucial for effective doping control and maintaining the integrity of the sports. This study explores the use of homogenized camel liver for detecting methandienone metabolites in camels. The biotransformation pathways of methandienone in homogenized camel liver tissues are analyzed using Liquid Chromatography-High Resolution Mass Spectrometry (LC-HRMS) to identify and characterize the phase I and phase II metabolites. Chromatographic separation was achieved using a Thermo-Hypersil C18 column. The study has identified 11 methandienone metabolites (M1-M11), this includes 10 phase I and one phase II metabolite. A glucuronic acid conjugate of methandienone was observed in this study, but no sulfonic acid conjugations were found. The metabolites and their possible chemical structures, along with their fragmentation patterns are confirmed using MSMS (MS2) experiments in data-independent acquisition (DIA) mode. These findings serve as a vital tool for the rapid detection of methandienone, combating its illicit use in camel racing. Comprehensive screenings covering both the parent drug and its metabolites are recommended to improve detection accuracy and ensure regulatory compliance in sports doping. Future research should explore methandienone's metabolite profile in administered camel samples.

Catalytic Advantages of SO3H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel-Crafts Acylation Reaction.

The catalytic activity and stability of sulfonic-based UiO-66(Zr) materials were tested in the Friedel-Crafts acylation of anisole with acetic anhydride. The materials were prepared using microwave-assisted synthesis, producing microporous materials with remarkable crystallinity and physicochemical features as acid catalysts. Different ratios between both organic ligands, terephthalic acid (H2BDC) and monosodium 2-sulfoterephthalic acid (H2BDC-SO3Na), were used for the synthesis to modulate the sulfonic content. The sulfonic-based UiO-66(Zr) material synthesized with a H2BDC/H2BDC-SO3Na molar ratio of 40/60 exhibited the best catalytic performance in the acidic-catalyzed Friedel-Crafts acylation reaction. This ratio balanced the number of sulfonic acid sites and their accessibility within the UiO-66 microporous structure. The catalytic performance of this material increased remarkably at 200 °C, outperforming reference acids and commercial heterogeneous catalysts such as Nafion-SAC-13 and Amberlyst-70. Additionally, the best sulfonic-based UiO-66(Zr) material proved to be stable in four successive reaction cycles, maintaining both its catalytic activity and its structural integrity.

Emulsion graft polymerization of glycidyl methacrylate onto bamboo fiber composites for efficient removal of lead ions from aqueous solutions

The emulsion graft polymerization process was used to synthesize a novel polyglycidyl methacrylate grafted silanized bamboo fiber composites. The grafting percentage was assessed by varying surfactant, initiator and monomer concentrations. The surface morphologies and thermal behavior of the biocomposites were analyzed using FTIR, SEM, XRD and TGA techniques. In batch adsorption studies, the effect of adsorption parameters like pH, adsorption time, adsorbent dose and solution temperature were examined on the adsorption efficiency of lead ions. The adsorption capacity of biosorbent composites was enhanced through conversion of epoxy group of Poly glycidyl methacrylate (PGMA) into sulfonic acid groups via sulfonation process. The sulfonic acid groups were incorporated into VMBF-g-PGMA by stirring the grafted sample in H2SO4 (98 %) for 2 h at 90 °C to obtain sulfonated grafted polymer (VMBF-g-PGMA-S). By increasing the concentration of monomers up to 5 %, the maximum grafting percentage (289 %) was achieved. The grafting % increases rapidly from 0.5 to 0.20 g initiator and at 0.20 g of initiator, the highest grafting yield was 512 %. The maximum Pb+2 adsorption capacity of adsorbent was 200 mg/g. The thermodynamic parameters for pb+2 adsorption revealed an exothermic and spontaneous nature of sorption process, and the entropy change showed that there are no substantial structural changes occurred in biosorbent material. The experimental results confirmed that sulfonated biosorbent composites are effective, economical, and promising adsorbent which could be used for removal of lead and other ions from aqueous solution.

Zwitterionic and vinyl-N-imidazolium ionic liquids

In this paper, we present employing our own and literature data the results of investigation of the thermal behavior and ion transport properties of vinyl and alkyl imidazolium zwitterions containing an alkane sulfonic acid group and salts on their basis. For comparison, we present the results of investigation the respective vinyl and alkyl imidazolium ILs without these functional groups. The phase behavior of zwitterionic and vinyl imidazolium ionic liquids is studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA).

Antibacterial effect of ultrasound combined with Litsea cubeba essential oil nanoemulsion on Salmonella Typhimurium in kiwifruit juice

This study investigated the antibacterial effect of ultrasound (US) combined with Litsea cubeba essential oil nanoemulsion (LEON) on Salmonella Typhimurium in kiwifruit juice and effect on the quality and sensory properties of kiwifruit juice. In this study, LEON prepared by ultrasonic emulsification method had a good particle size distribution and high stability. The US+LEON treatment significantly (P < 0.05) improved antibacterial efficacy, compared to the control, and would not destroy the nutritional components containing ascorbic acid, flavonoids, total phenol and total soluble solids. Meanwhile, US+LEON treatment enhanced 2, 2-diphenyl-1-picrylhydrazyl (DPPH), 2, 2′-azino-bis-(3-ethylbenzothiazoline-6 sulfonic acid) (ABTS) radical scavenging capacity and ferric ion reducing antioxidant power (FRAP). In terms of sensory properties, US and LEON had a significant (P < 0.05) effect on the odor and overall morphology of kiwifruit juice. The enhance of antibacterial efficacy and the retention of nutrients by combined treatments shows that US+LEON is a promising antibacterial method that will provide new ideas for the processing and safety of fruit juices, and the US parameters and LEON concentration should be adjusted to reduce the effect on food sensory properties in future studies.

Synthesis and Density Functional Theory Study on the Functionalization of Carbon Nanotube Conjugates with Amino Compounds and Their Application in Dyeing Processes

AbstractThis study investigates the functionalization of graphene nanotube (GNTs) conjugates with an amino compound called 1‐amino‐2‐hydroxy‐4‐naphthalene sulfonic acid (AHNSA‐GNTs). The study also evaluates the potential application of these conjugates in dyeing processes. The goal is to modify GNTs to enhance their interaction with dyes, thus improving the efficiency of dyeing textiles and the colorfastness of the resulting products. Multiple characterization methods, such as X‐ray diffraction (XRD), scanning electron microscopy (SEM), and atomic force microscopy (AFM) were used to get a better look at the composites. The findings of the study indicate that AHNSA‐GNTs composites improve dye retention on wool fibers, which leads to a reduction in the consumption of excess dye and water. Density Functional Theory (DFT) calculations were utilized to investigate the electronic properties and binding energies of the functionalized CNTs, providing insights into the molecular interactions between the CNTs and amino compounds. Overall, this study highlights the promising applications of graphene nanotubes in sustainable textile processes. Frontier molecular orbitals (FMOs) and global reactivity descriptors serve as key tools for understanding the stability and chemical reactivity of compounds. These tools were used to calculate FMOs and electronic parameters of compounds 1 and 2 at the B3LYP/6‐31G(d) level of theory. The study examined the highest occupied molecular orbital (HOMO)‐lowest unoccupied molecular orbital (LUMO) energy gap, which provides insights into molecular stability and reactivity. Various physical properties were derived from these calculations, including electron affinity (EA) and ionization potential (IP) to LUMO and HOMO energies. Compound 2 emerged as the most efficient electron donor, possessing the highest HOMO energy, while compound 1 excelled as the best electron acceptor with the highest LUMO energy.