Zeta Potential Analysis Research Articles

Polymeric Nanodiscs Comprising 5-Fluorouracil for Inhibition of Protein Aggregation and Their Anti-Alzheimer's Activity in the Drosophila Model.

Nanoconjugates are promising for therapeutic drug delivery and targeted applications due to the numerous opportunities to functionalize their surface. The present study reports the synthesis of 5-fluorouracil (5-FU)-entrapped polyvinylpyrrolidone (PVP) nanoconjugates, precisely 5-FU-PVP and 5-FU-PVP-Au, and the evaluation of protein aggregation inhibition efficiency. The 5-FU-loaded polymer nanoconjugates were functionalized with gold nanoparticles and analyzed using characterization techniques like dynamic light scattering, UV-visible spectroscopy, Fourier-transform infrared spectroscopy, and zeta potential analysis. These conjugates exhibit consistent morphology with a spherical, flat, disc-like structure. The 5-FU-PVP and 5-FU-PVP-Au nanoconjugates exhibited a high drug loading, up to 81% and 90%, respectively. The nanoconjugates exhibited prolonged drug delivery of 5-FU from 5-FU-PVP and 5-FU-PVP-Au, wherein 5-FU-PVP-Au depicted a higher drug release. They were investigated for inhibiting the protein hen egg white lysozyme (HEWL) aggregation by ThT fibril size measurement, binding assay, and electron microscopy, and the results showed that conjugates repressed the fibrillogenesis in HEWL. The prominent activity of amyloid aggregation inhibition for HEWL using 5-FU-PVP and 5-FU-PVP-Au was found to be 29 μg.mL-1 and 27 μg.mL-1, respectively. The dissociation of amyloid aggregates was achieved against 5-FU-PVP and 5-FU-PVP-Au at 27 μg.mL-1 and 25 μg.mL-1, respectively. Furthermore, the nanoconjugates were investigated for anti-Alzheimer's activity in the Drosophila model. A Drosophila model of Alzheimer's disease (AD) was developed that expressed Aβ42 peptides in the neuronal secretory system to comprehend the pathogenic effects of Aβ42 in vivo. All the results demonstrate that polymer nanoconjugates exhibit more effective inhibition of protein aggregation than bare drugs.

Biomimetic niosomal versus liposomal nanoparticle-based aspirin injection for treating stroke and myocardial infarction.

In this work, we are comparing biomimetic niosomal nanoparticles (BNNs) with biomimetic liposomal nanoparticles (BLNs) and studying their drug carrier properties. A-BNNs and A-BLNs are prepared by lipid hydration method and characterized using DLS for size and zeta potential analysis, surface morphology by SEM, structural details by TEM, crystallinity and phase change by XRD, thermodynamic properties by DSC, TGA and DTGA, drug carrier properties by entrapment efficiency, drug release studies by open-end tube method and its mechanistic assessment by fitting with various models such as zero order, first order, Higuchi and Korsmeyer-Peppas models. The A-BNNs had an average size of 157.0 ± 3.58nm and A-BLNs had an average size of 173 ± 1.24nm. The A-BNNs had an average zeta potential of -29.0 ± 1.11mV and A-BLNs had an average zeta potential of -46.5 ± 1.11mV. The A-BNNs have an average entrapment efficiency of 94 ± 0.4% and A-BLNs have an average entrapment efficiency of 98 ± 0.14%. The BNNs have an average drug release of 78.12 ± 1.57% and A-BLNs have an average release of 98.41 ± 1.87% over 24hours. Our results show that the vesicular size dependence influences the resulting nanoparticle drug carrier properties. This is a robust demonstration of the phenomena at the nanoscale that the precursor vesicular system size dependency will be reflected in bulk-engineered nanoparticle properties. These novel nanoparticles are potential candidates for development as an injection to suppress clots in stroke and myocardial infarction.

Pyrite depression by sodium metabisulfite and dextrin with xanthates: contact angle, floatability, zeta potential and IR spectroscopy studies

The individual and combined depressive action of metabisulfite and dextrin on pyrite in the presence and absence of amyl xanthate has been studied through contact angle, zeta potential, microflotation, and IR spectroscopy analyses. The combined application of depressants significantly reduces the contact angle of pyrite compared with that of galena, with this effect being enhanced when the pulp is oxygenated during conditioning with metabisulfite, facilitating pyrite surface oxidation. Zeta potential measurements demonstrate the role of the oxidation process in decreasing the magnitude of the negative electric charge on the pyrite surface. These results were further corroborated by IR spectroscopy studies, which confirmed the oxidation of the pyrite surface in the presence of metabisulfite, as well as the co-adsorption of dextrin and amyl xanthate. In microflotation experiments, pyrite and galena exhibited contrasting flotation behaviors, with pyrite being effectively depressed at pH 8 when a combination of air, metabisulfite, and dextrin was used.

Antimicrobial activity and cytotoxic and epigenetic effects of tannic acid-loaded chitosan nanoparticles

Tannic acid (TA) is a potent antitumor agent, but its low bioavailability and absorption limit its use. In this study, it was loaded into chitosan-based nanoparticles (Chi-NPs) to overcome these limitations and to improve its antimicrobial and anticancer activities. TA-loaded Chi-NPs (Chi-TA-NPs) were synthesized using the ionic gelation method and physicochemically characterized by FE-SEM, FTIR, XRD, PDI, DLS, and zeta potential analysis. Additionally, the antimicrobial activity of Chi-TA-NPs against two G+ bacterial strains, two G− bacterial strains, and a fungal strain (Candida albicans) was investigated using the microbroth dilution method. MTT assay was used to examine the cytotoxic effects of Chi-TA-NPs on HepG2 cells. The expression of DNA methyltransferase 1 (DNMT1), DNMT3A, and DNMT3B was examined in HepG2 cells using RT-qPCR. The amount of 5-methylcytosine in the HepG2 cell-derived genomic DNA was measured using ELISA. FE-SEM micrographs showed the loading of TA into the chitosan-based formulation. The peaks detected in the XRD and FTIR analyses confirmed the formation of the Chi-TA-NPs. The PDI value (0.247 ± 0.03), size (567.0 ± 25.84 nm), and zeta potential (17.0 ± 5.86 mV) confirmed the relative stability of Chi-TA-NPs. A constant release profile in line with the Korsmeyer-Peppas model was detected for Chi-TA-NPs, such that approximately 44% of TA was released after 300 min. In addition, Chi-TA-NPs exhibited effective antimicrobial activity against the studied microbial strains, as manifested by MIC values ranging from 250 to 1000 µg/mL. Chi-TA-NPs induced cytotoxicity in liver tumor cell line, with an IC50 value of 500 µg/mL. Furthermore, Chi-TA-NPs considerably decreased the expression of DNMT1 (2.52-fold; p = 0.01), DNMT3A (2.96-fold; p = 0.004), and DNMT3B (2.94-fold; p < 0.0001). However, 5-methylcytosine levels in HepG2 cells were unaffected by Chi-TA-NPs treatment (p = 0.62). Finally, the antimicrobial, cytotoxic, and epigenetic effects of Chi-TA-NPs were more pronounced than those of free TA and the unloaded Chi-NPs. In conclusion, Chi-TA-NPs exhibit promising potential for reducing microbial growth and promoting cytotoxicity in liver cancer cells.

Phycogenic nanoparticles efficiently catalyse pesticide degradation through a novel metabolic pathway utilizing solar light

Cypermethrin (Cy) is a widely used insecticide, leading to significant environmental contamination in homes and agricultural areas. Effective methods to minimize or eliminate insecticidal residues are essential. Seaweeds, traditionally used in agriculture as soil conditioners, offer a promising solution for remediating pesticide-contaminated soils through biogenic nanoparticle synthesis. In this study, we synthesized biogenic silver nanoparticles (UL-AgNPs) from the green seaweed Ulva lactuca Lin (Ulvaceae) to degrade Cypermethrin. The UL-AgNPs were characterized using UV-Visible spectroscopy, Scanning Electron Microscopy equipped with Energy dispersive X-ray spectroscopy, Fourier Transform Infra-red spectroscopy, X-ray diffraction, Dynamic light scattering and zeta potential analysis, confirming their presence, size (81.29 nm), structure and stability. Response surface methodology (RSM) was used to assess the catalytic concentration of photocatalyst for degradation of pesticide including variables, Cy concentration and destined exposure time duration. The degradation efficiency of UL-AgNPs was evaluated, with the highest degradation (91.2%) achieved at pH 7 after 12 hours using 16.6 mg L-1 of UL-AgNPs, following pseudo-first order kinetics with a rate of 2.7 hour-1. GC-MS and UV-Visible spectroscopy revealed a novel degradation pathway, where Cypermethrin was broken down into compounds like Tetradecane, Dodecane, and Tetracosanoic acid through ester cleavage and benzene ring breakdown. The study also demonstrated the reusability of UL-AgNPs for four cycles, highlighting their potential for sustainable environmental management by reducing the long-term hazards of Cypermethrin.

Synthesis, modification, characterization, and in vitro evaluation of chitosan-hyaluronic acid coated MIL-100 (Fe) nanoparticles for methotrexate delivery in rheumatoid arthritis.

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by inflammation of the joints, leading to pain, swelling, and potential joint destruction. Effective management of RA is crucial to improve patients' quality of life and prevent long-term disability. Methotrexate (MTX) is a widely used disease-modifying antirheumatic drug (DMARD) that has shown efficacy in treating RA. However, its use is often limited by significant adverse effects, particularly on healthy tissues and organs, including hepatotoxicity, myelosuppression, and gastrointestinal complications. Therefore, developing targeted drug delivery systems (DDSs) for MTX is essential to enhance its therapeutic effects while minimizing systemic toxicity. Metal-organic frameworks (MOFs), specifically MIL-100(Fe), present a promising approach for targeted drug delivery in RA treatment due to their high porosity, large surface area, and excellent loading capacity. The acid-responsive properties of MIL-100(Fe) make it particularly suitable for targeting the acidic microenvironment of inflamed joints. In this study, we synthesized MIL-100(Fe) using a microwave-assisted method and embedded MTX within these nanocarriers. The nanocarriers were subsequently coated with chitosan and modified with hyaluronic acid through 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC). Comprehensive characterization techniques such as dynamic light scattering (DLS), zeta potential analysis, Brunauer-Emmett-Teller (BET) surface area measurement, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and field emission scanning electron microscopy (FESEM) were employed to evaluate the nanoparticles. Additionally, we assessed cell cytotoxicity and cellular uptake in macrophage cell lines. Overall, the results indicate that the prepared MIL-100(Fe) nanoparticles are a suitable DDS for targeted MTX delivery in RA treatment.

Synthesis and characterization of a copper-based metal–organic framework and its application in microextraction and determination of chlorpyrifos by ion mobility spectrometry

This study describes an innovative method for the microextraction and determination of chlorpyrifos, utilizing a newly synthesized copper-based metal–organic framework (MOF) with 3,3ʹ-thiodipropionic acid as the ligand. This approach offers a sensitive and reliable solution for the ultra-trace determination of chlorpyrifos in various matrices, highlighting its potential for broader environmental and food safety applications. To minimize environmental impact, a hydrothermal method was chosen for MOF synthesis. The MOF was fully characterized using FT-IR, X-ray diffraction, FESEM-EDX, BET, zeta potential analysis, and XPS; and integrated into a dispersive solid-phase microextraction (DSPME) technique, paired with ion mobility spectrometry (IMS) for chlorpyrifos detection. The DSPME procedure has been optimized for extraction efficiency, minimal solvent use, and low absorbent consumption. A low detection limit of 0.65 ng mL−1 was observed and validated along with a linear detection range of 1.0–400.0 ng mL−1 as the result of this optimization. Experiments with water, pear fruit, and soil samples demonstrated the method’s practicality and superior performance compared to existing techniques, showcasing its potential for real-world applications.

Green synthesis of silver nanoparticles from supercritical CO2 mediated Lagerstroemia speciosa extract: Characterization, antimicrobial and antibiofilm activity

In the current study, optimal supercritical fluid extract (SFE) of Lagerstroemia speciosa (LS) leaves at pressure 29.59 megapascal (MPa), temperature 89.50 ºC and extraction time 53.85 min. was used to extract phenolic compounds for the synthesis of silver nanoparticles (AgNPs). The synthesis was studied for 0-20 hrs. Initially the synthesis of nanoparticles (SFELS-AgNPs) was confirmed using UV -spectroscopy. It demonstrated a maximum surface plasmon resonance at 430 nm. The crystallite dimension of nanoparticles was determined using X-ray diffraction (XRD) (13.47 nm), Transmission electron microscopy (TEM), zeta potential analysis and energy-dispersive X-ray analysis (EDAX) were used to analyze the morphology, surface charge and presence of differential elements in SFELS-AgNPs respectively. Developed nanoparticles revealed antimicrobial activity against two gram-positive viz. Staphylococcus aureus and Bacillus cereus, and three gram-negative bacteria viz. Klebsiella pneumonia, Pseudomonas aeruginosa and Escherichia coli. The nanoparticle showed a minimum inhibitory concentration (MIC) of 64 μg/ml whereas the minimum bactericidal concentration (MBC) 128 μg/ml against K. pneumonia. They significantly inhibited K. pneumonia biofilm formation which was confirmed using scanning electron microscopy (SEM). The results were encouraging compared to the standards drug Chloramphenicol and other controls. The generated nanoparticles have highly effective antimicrobial properties against pathogenic bacteria.

Salvia sclarea L. (Clary Sage) Flower Extract-Mediated Green Synthesis of Silver Nanoparticles and Their Characterization, Antibacterial, Antifungal, and Scolicidal Activities against Echinococcus granulosus

Over the past few decades, nanoscience has gained a prominent position in plant-mediated synthesis of nanoparticles due to its advantages, such as environment-friendly and practical nature and biological safety and compatibility. This study was conducted to develop silver nanoparticles (NPs) based on Salvia sclarea flower extract and characterize them using UV-visible spectroscopy, Dynamic Light Scattering, Zeta potential analysis, Fourier Transform Infrared Spectroscopy, X-ray diffraction, Field Emission Scanning Electron Microscopy, and Transmission electron microscopy. We also evaluated the antibacterial (4 standard bacterial strains), anti-Candida (40 clinical isolates), and scolicidal activities of the green-synthesized Ag NPs. The characteristic absorption peak at 440nm indicated the successful synthesis of AgNPs with spherical morphology and a size range of 30-40nm according to TEM imaging. The FT-IR spectrum revealed the presence of functional constituents such as phenols, terpenoids, and saponins in the flower extract that could reduce metal ions and form AgNPs. EDX analysis confirmed the presence of silver (91.3%) in the synthesized NPs. In addition, AgNPs exhibited remarkable antimicrobial activity. The highest antibacterial and antifungal activities of AgNPs were observed against Bacillus cereus and Candida krusei, respectively, while the lowest activities were observed against Pseudomonas aeruginosa and Candida albicans. At the concentration of 320μg/mL, AgNPs delivered the highest percentage of mortality (100%) against liver hydatid cyst protoscoleces within 15minutes. Our findings highlight the potential of S. sclarea extract as an inexpensive and readily available material for producing biogenic AgNPs with versatile applications.

Surface tension of graphene/Fe3O4 water-based hybrid nanofluids

Advanced hybrid nanofluids have been engineered through the synthesis of aqueous suspensions containing graphene sheets and iron oxide (Fe3O4) nanoparticles at a graphene-Fe3O4 mass ratio of 70:30. Karaya gum and cocoamidopropyl betaine (CAPB) were selected as surfactants given their good affinity with dispersed nanomaterials. Graphene sheets with Fe3O4 nanoparticles as well as the prepared dispersions were first characterized in terms of morphology, chemical composition and stability using various techniques, including electron microscopy, UV–visible spectroscopy and Zeta potential analyses. Given the crucial role that surface tension (ST) plays in boiling/condensation processes or micro-flow applications, this physical property was investigated at nanoadditive mass concentrations of 0.005–0.100 % and temperatures of 283.15–313.15 K using the pendant drop method. As an entry parameter for ST evaluation, the density of these hybrid nanofluids was also measured at the same temperature and concentration ranges. Experimental studies revealed that ST of water reduces with the addition of surfactant and increasing temperature. Graphene-Fe3O4 nanoparticles were also found to further reduce the ST (thus enhancing the effect of the surfactant mixture) by up to 42.7 % on average at 0.1 %wt. compared to water in the tested temperature range. This may be potentially interesting for improving boiling heat transfer performance and optimizing bubble flow pattern.

Coagulative removal of polyethylene microplastics using polyaluminum chloride in conjunction with laminarin

As emerging pollutants in water, microplastics pose potential risks to aquatic organisms and human health. Previous studies have shown that traditional metal coagulants are effective in removing microplastics from water, but they come with drawbacks such as high chemical dosage and metal residues. Therefore, it is important to explore more efficient coagulation systems. This study utilized laminarin (LA) as a coagulant aid in combination with polyaluminum chloride (PAC) to investigate its enhanced coagulation performance on polyethylene microplastics in water. The performance of coagulation systems for the removal of microplastics was evaluated for different agent dosages, pH, anion and HA content. Experimental results demonstrated that the compounded system (PAC-LA) significantly improved the removal efficiency of PE microplastics compared to the single PAC system, achieving a removal rate of 91.5% while reducing the dosage of PAC. The enhanced coagulation mechanism of LA was analyzed using various techniques including scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and zeta potential analysis. The results indicated that charge neutralization and sweep flocculation were the primary coagulation mechanisms in the presence of PAC alone. The effect of charge neutralization and adsorption was strengthened with the introduction of LA. The coagulation system of PAC-LA showed higher removal rates of PE microplastics under different environmental conditions such as varying pH levels, co-existing anions, and humic acid, suggesting a promising application for microplastic control in water.

Ultraviolet (UV) assisted fabrication and characterization of lignin containing cellulose nanofibrils (LCNFs) from wood residues.

This study aimed to explore the synergistic mechanism of lignin chromophore modifications via UV treatment and to analyze the effects of mechanical treatments on LCNF properties for future uses. The procedure involved two steps: first, lignin's chromophore modification via UV illumination, and then the ball milling process was proceeded for 1 h, followed by high-intensity ultrasonic for 15-135 min. Characterization included preserved lignin content percentage, FTIR, UV-vis NMR, and color analysis for UV-modified samples, and to access the influence of mechanical treatment on LCNF samples further yield, zeta potential analysis, XRD, thermogravimetric analysis, atomic force microscopy, and scanning electron microscopy were performed. LCNFs S-120 demonstrated a zeta potential of -21.7 mV, indicating enhanced stability compared to the S-135 sample (-10.95 mV). The S-120 sample also showed the highest yield (74.02 %) and TGA at 391 °C. In XRD analysis, the S-120 sample demonstrated the highest CrI 64.3 %, than the S-15 sample (48.2 %). Preserved lignin in the LCNFs led to a slight reduction in crystallinity across all samples but improved thermal stability for all the prepared LCNFs samples. The UV and ultrasonication improved the homogeneity and durability of the LCNF samples, enabling a process that may be used to industries.

Pea protein-p-coumaric acid conjugate-based antioxidant film: The relationship between protein structure and film properties after covalent bonding

In this study, pea protein isolates (PPI) have been used to make conjugates by covalent binding with p-coumaric acid (p-CA), and the effect of conjugation on PPI structural characteristics and the structural, optical, mechanical, and physicochemical properties of conjugate-based films were investigated. The conjugation with p-CA unfolds the tertiary structure of PPI and significantly reduces the surface charge. A tendency of aggregation with increasing p-CA addition was proposed. The conjugate-based films show stronger tensile strength (TS) and better water barrier properties than PPI-based films. However, no significant improvement of the elongation at break (EAB) and thermal stability was found for conjugate-based films. FTIR spectroscopic and zeta-potential analyses indicated that such improved film properties could be attributed to the enhancement of hydrogen bonds and weakening of electrostatic repulsion between conjugate-conjugate. Additionally, the conjugates impart the antioxidant activity to the films as confirmed by DPPH scavenging capacity. This study demonstrates the potential of using pea protein-phenolic acid conjugate to make PPI-based films with improved mechanical properties, water barrier properties, and antioxidant activity.

High-performance copper terephthalic acid metal-organic framework/gum Arabic/carrageenan composite beads for efficient lead(II) removal from aqueous solutions

Lead (Pb(II)) contamination poses a significant threat to human health and the environment. This study investigates a new approach for Pb(II) removal from polluted water using copper terephthalic acid metal-organic framework/gum Arabic/potassium carrageenan (MGC) composite beads. We synthesized copper terephthalic acid MOF, potassium carrageenan beads, and MGC composite beads to evaluate their adsorption potential. Characterization of the synthesized adsorbents was performed using TGA, nitrogen adsorption/desorption, ATR-FTIR, zeta potential, SEM, and TEM analyses, revealing that MOF > MGC > KG in thermal stability. The MGC composite exhibited a high specific surface area (398.03 m2/g) with mesopores and diverse functional groups, alongside a pH of zero point charge (pHpzc) of 6.8 and a small particle size (20 nm). The maximum Langmuir adsorption capacity for Pb(II) removal by MGC reached 374.7 mg/g under optimized conditions (20 °C, pH 5, 60 min shaking time, 3.0 g/L adsorbent dosage). The adsorption data fit well with the Pseudo-First-Order kinetic model and Langmuir and Dubinin-Radushkevich isotherm models. The adsorption process was physical, favorable, and endothermic. EDTA was used as a desorption agent, showing that the composite beads retained 97 % efficiency after ten cycles, highlighting MGC's potential as a sustainable strategy for Pb(II) remediation.

Implementation of Silver Nanoparticles Green Synthesized with Leaf Extract of Coccinia grandis as Antimicrobial Agents Against Head and Neck Infection MDR Pathogens.

Head and neck infections (HNI) associated with multidrug resistance (MDR) offer several health issues on a global scale due to inaccurate diagnosis. This study aimed to identify the bacteria and Candidal isolates and implement the silver nanoparticles green synthesized with leaf extract of Coccinia grandis (Cg-AgNPs) as a therapeutic approach against HNI pathogens. The Cg-AgNPs were characterized by the UV-visible spectrophotometer, FT-IR analysis, Zeta particle size, Zeta potential, and field emission scanning electron microscope (FESEM) analysis to validate the synthesis of nanoparticles. Additionally, the antimicrobial activity of Cg-AgNPs was presented by the zone of inhibition (ZOI), minimum inhibitory concentration (MIC), minimum bactericidal/fungicidal concentration (MBC/MFC), and antibiofilm assay. Moreover, the cell wall rupture assay was visualized on SEM for the morphological study of antimicrobial activities, and the in-vivo toxicity was performed in a swiss mice model to evaluate the impact of Cg-AgNPs on various biological parameters. Different bacterial strains (Staphylococcus aureus, Acinetobacter baumannii, Klebsiella pneumoniae, and Pseudomonas aeruginosa) and Candida sp. (Candida albicans, Candida tropicalis, Candida orthopsilosis, and Candida glabrata) were identified. The MIC, MBC, and antibiofilm potential of Cg-AgNPs were found to be highest against A. baumannii: 1.25 μg/ml, 5 μg/ml, and 85.01±5.19% respectively. However, C. albicans and C. orthopsilosis revealed 23 mm and 21 mm of ZOI. Subsequently, the micromorphology of the cell wall rupture assay confirmed the efficacy of Cg-AgNPs, and no significant alterations were seen in biochemical and hematological parameters on the swiss mice model in both acute and subacute toxicity studies. The green synthesized Cg-AgNPs have multifunctional activities like antibacterial, anticandidal, and antibiofilm activity with no toxicity and can be introduced against the HNI pathogens.

The Inhibitory Effect of Low Phosphorus and Low Molecular Weight Terpolymer Scale Inhibitor on Calcium Scale in Oilfields

ABSTRACTThe study utilized itaconic acid (IA), N‐hydroxyethyl acrylamide (HEAA), and sodium hypophosphite (SHP) as starting materials for a free radical polymerization process. This process resulted in creating a new type of low‐phosphorus terpolymer scale inhibitor called P(IA‐HEAA‐SHP). Its primary application was as an effective scale inhibitor to block CaCO3 and CaSO4. FTIR, 1H‐NMR, and 13C‐NMR were used to characterize the synthesized copolymer structures, and it was confirmed that the synthesized products had the desired structures. The synthesis conditions have been optimized using the static scale inhibition approach, which involved adjusting the monomer ratio, initiator dosage, and reaction time. This resulted in the synthesis of polymeric scale inhibitors with outstanding scale inhibition properties. Additionally, GPC was employed to examine the correlation of the molecular weight of the polymers with their scale inhibition properties at various reaction times. The results showed that when the monomer ratio n(IA):n(HEAA) = 1.5:1, the SHP dosage mass fraction was 15%, the ammonium persulfate initiator dosage was 10%, the reaction temperature was 90°C, and the reaction time was 4 h. At a measured dose of 30 mg L−1, the scale inhibition impact on CaCO3 is 86.63%, while the scale inhibition impact on CaSO4 is 96.83%. The thermal properties of the copolymers, the crystal structure, and the micro‐morphology of the scale samples were analyzed by TGA, XRD, and SEM, and the scale inhibition mechanism was discussed in conjunction with the zeta potential analysis.

Green Biosynthesis of Silver Nanoparticles using Aqueous Extract of Pseuderanthemum reticulatum Leaves and their Antioxidant and Anti-Aging Activities

The plant based synthesis of nanoparticles are highly recommended because of its low toxicity, low cost and eco-friendly nature. In present work, synthesis of silver nanoparticles (AgNPs) involves a bioreduction technique using the aqueous extract derived from the leaves of Pseuderanthemum reticulatum. The synthesized AgNPs were characterized by UV-visible, FT-IR, EDAX, XRD, SEM, TEM, zeta potential analysis and particle size analyzing techniques. The results showed the characteristic absorbance peak at 404 nm in the UV-visible spectrum, the strong signals observed in the EDAX spectrum and the other characterization confirmed the formation of AgNPs with an average particle size of 17.83 nm. The in vitro antioxidant activity of AgNPs by DPPH method results revealed that they have greater radical scavenging capacity with the IC50 value of 101.5 µg/mL. Additionally, the anti-aging activity was also determined by collagenase inhibition assay. The biogenic AgNPs established its strong anti-aging efficacy as demonstrated by their inhibitory capacity against Actinomyces israelii (collagenase enzyme). Since, the AgNPs synthesized using aqueous extract of P. reticulatum exhibited leaves excellent antioxidant and anti-aging activity, it can be promising choice for various biological applications.

A novel eco-friendly depressant Scutellaria Baicalensis Extract SBE and its performance on flotation separation of chalcopyrite from sphalerite: A combined experimental and mechanism investigation

This research investigates the utilization of Scutellaria Baicalensis Extract (SBE) as a depressant in the flotation separation of sphalerite and chalcopyrite with Potassium Amylxanthate (PAX) serving as the flotation collector. The feasibility of SBE as a sphalerite depressant at near neutral pH conditions was evaluated through flotation tests, and its depression mechanism was explored using contact angle measurements, zeta potential measurements, adsorption measurements and XPS analyses. Micro-flotation experiments demonstrated the efficacy of SBE as a sphalerite depressant. In artificial mixed mineral experiments, a Cu concentrate with a recovery of 92.55 % and a grade of 28.45 % Cu, and a Zn concentrate with a recovery of 94.43 % and a grade of 57.30 % Zn were obtained at an SBE concentration of 37.5 mg/L. Contact angle, zeta potential and adsorption measurements revealed that SBE was adsorbed onto both sphalerite and chalcopyrite surface, with stronger adsorption on sphalerite. The amount of SBE adsorption on sphalerite exceeded that on chalcopyrite, and SBE prevented the collector’s adsorption on sphalerite while minimally affecting chalcopyrite. XPS analysis results suggested that SBE likely acts through physical adsorption on the mineral surface.

Cooperative effects of quaternary ammonium salt collectors and cationic polyacrylamide on flotation separation of diaspore and kaolinite: Experimental study and simulation

In the presence of depressant cationic polyacrylamide (CPAM), three quaternary ammonium salt as collectors were used in the flotation separation of diaspore and kaolinite, respectively. The flotation results of single minerals showed that the high recovery of the kaolinite and the low recovery of diaspore were gained, which indicated that the floatability of kaolinite was hardly affected while the floatability of diaspore was obviously weakened by using Gemini collector and CPAM under the conditions of pulp pH value of 6. The mass ratio of Al2O3 to SiO2 (A/S) was also increased from 4.86 to 8.90. FTIR spectra, adsorption capacity of collectors and zeta potential analysis illustrated that the maximum difference value in adsorption capacity of Gemini collector on the surface of kaolinite and diaspore was obtained because of the differences of the collectors in the presence of CPAM. This phenomenon was further supported by molecular dynamics simulation analysis and XPS analysis. The opinion can be provided that the difference between kaolinite and diaspore was enlarged by regulating the cooperation of the collector and the depressant for increasing the flotation separation of minerals.

High efficiently removal of Cd(II) in environmental water samples by nano-particle supported ionic liquid material

Ionic liquids have been considered as green solvent for metal ion extraction. However, the high cost, low efficiency and hard phase separation limit their application. In this work, nano SiO2 supported ionic liquid (SiO2@NH-IL) prepared via simple homogeneous sol-gel method was used for adsorptive removal of Cd(II) from water sample. The material was characterized by XRD, TEM and FT-IR and zeta potential analysis. The adsorption kinetics, adsorption isotherm and reusability as well as the adsorption mechanism were investigated. The effects of solution pH and temperature were also studied. It was found that this nano-adsorbent could be used to remove trace level of Cd(II) efficiently due to the strong coordination of Cd(II) with the ionic liquid. Thermodynamic and kinetic studies showed that the adsorption rate increased with the increase of temperature, the maximum adsorption capacity was 112.13 mg g−1 at higher temperature (i.e. 80 °C), and the adsorption equilibrium could achieve in 30 min. The nano-adsorbent could be easily regenerated by 0.5 mol L−1 of HCl and reused as least ten adsorption/desorption cycles. The as-prepared nano-adsorbent are potential candidate for adsorptive removal of Cd(II) in polluted wastewater, especially with higher temperature.