Adsorption of oxytetracycline on kaolinite.
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ABSTRACT:
SUBMITTER: Song Y
PROVIDER: S-EPMC6857953 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:The discharge of antibiotics and the potential threat to organisms posed by this have received increasing attention. In this work, flocculent magnesium silicate (FMS) was fabricated by a facile hydrothermal and freeze-drying process, and its adsorption behavior for antibiotic oxytetracycline (OTC) was investigated. FMS presented a sepiolite-type structure and the alkaline solution promoted its hydroxylation. A hierarchical pore structure ranging from micropores to macropores and a high specific surface area of 660 m2/g were exhibited. FMS exhibited a higher adsorption amount in neutral solution than in acidic or alkaline conditions as the physicochemical properties of FMS and OTC were significantly affected by the pH. Adsorption isotherm could be well-described by the Langmuir model, and the calculated saturated adsorption capacity was as high as 265 mg/g. Adsorption kinetics followed the pseudo-second-order kinetic model, and the adsorption rate-controlling step was intraparticle diffusion. Thermodynamic parameters indicated that the adsorption was a spontaneous physicochemical reaction. After five cycles, around 91% of the adsorption performance was still maintained, demonstrating the excellent reusability of FMS. The sepiolite-type FMS fabricated in this work could be applied to remove OTC from wastewater.
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Project description:The adsorption of bixin in aprotic solvents onto acid- and alkali-treated kaolinite was investigated. Kaolinite was treated three times, for 6?h each, with 8?M HCl or 5?M KOH. The adsorbents were characterized by XRD, FT-IR, EDS, and BET-N2. The effects of contact time and dye concentration on adsorption capacity and kinetics, electronic transition of bixin before and after adsorption, and also mechanism of bixin-kaolinite adsorption were investigated. Dye adsorption followed pseudo-second order kinetics and was faster in acetone than in dimethyl carbonate. The best adsorption results were obtained for KOH-treated kaolinite. In both of the solvents, the adsorption isotherm followed the Langmuir model and adsorption capacity was higher in dimethyl carbonate (qm ?=?0.43?mg/g) than in acetone (0.29?mg/g). The adsorption capacity and kinetics of KOH-treated kaolinite (qm ?=?0.43?mg/g, k2?=?3.27?g/mg·min) were better than those of HCl-treated kaolinite (qm ?=?0.21?mg/g, k2?=?0.25?g/mg·min) and natural kaolinite (qm ?=?0.18?mg/g, k2?=?0.32?g/mg·min). There are shift in the band position of maximum intensity of bixin after adsorption on this adsorbent. Adsorption in this system seemed to be based essentially on chemisorption due to the electrostatic interaction of bixin with the strong basic and reducing sites of kaolinite.
| S-EPMC5822873 | biostudies-literature
Project description:This work aimed at studying the potentiality of interactions between kaolinite surfaces and a protein-fragment (350-370 amino acid units) extracted from the glycoprotein E1 in the transmembrane domain (TMD) of hepatitis C virus capsid. A computational work was performed for locating the potential electrostatic interaction sites between kaolinite aluminol and siloxane surfaces and the residues of this protein-fragment ligand, monitoring the possible conformational changes. This hydrated neutralized kaolinite/protein-fragment system was simulated by means of molecular modeling based on atomistic force fields based on empirical interatomic potentials and molecular dynamic (MD) simulations. The MD calculations indicated that the studied protein-fragment interacted with the kaolinite surfaces with an exothermic process and structural distortions were observed, particularly with the hydrophilic aluminol surface by favorable adsorption energy. The viral units isolation or trapping by the adsorption on the kaolinite nanoparticles producing structural distortion of the peptide ligands could lead to the blockage of the entry on the receptor and hence a lack of viral activity would be produced. Therefore, these findings with the proposed insights could be an useful information for the next experimental and development studies in the area of discovering inhibitors of the global challenged hepatitis and other pathogenic viruses based on the phyllosilicate surface activity. These MD studies can be extended to other viruses like the COVID-19 interacting with silicate minerals surfaces.
| S-EPMC7556793 | biostudies-literature
Project description:In this paper, groundwater treatment sludge (GTS) was recycled as a magnetic adsorbent via a facile calcination process without adding any reductant. The prepared magnetic adsorbents (MAs) were characterized by scanning electron microscopy (SEM), X-ray diffractometer (XRD) and X-ray photoelectron spectroscopy (XPS), vibrating sample magnenometer (VSM) and Mössbauer spectroscopy. The results showed that GTS comprised 33.2% Fe, 1.4% Al and 6.2% Si, and exhibited a weak saturation magnetization of 0.0008 emu/g. Without NaOH, the GTS calcinated at 700 and 500 °C were well magnetized with Ms of 20.1 and 7.1 emu/g, separately, but exhibited a low Ms of 0.43 emu/g at 300 °C. By adding NaOH powder, the Ms of GTS apparently increased to 4.9 emu/g after calcination at 300 °C, and further to 8.5 emu/g at 500 °C. In GTS, about 96.1% Fe was involved in ferrihydrite form. The Ms of calcinated GTS was accompanied with the phase transformation of ferrihydrite to maghemite. Si/Al oxides in GTS coordinated on the surface sites of ferrihydrite and inhibited the conjunction and phase transformation of adjacent ferrihydrite particles, but were effectively desorbed as in the presence of NaOH. Na500, preparing by calcinating GTS at 500 °C with NaOH, showed an optimal total surface sites (Hs) of 0.65 mmol/g. Oxytetracycline (OTC) was used as a target for studying the adsorption characteristics of synthetic magnetic adsorbents and a high adsorption capacity of oxytetracycline of 862.1 mg/g in comparison with the other calcinated GTS, and the adsorption data was consistent with the Langmuir model. By adding 6 g/L Na-500, approximately 100% of oxytetracycline and tetracycline and nearly 40% total organic carbon were removed from real pharmaceutical wastewater. With the method, GTS can be converted in mass production to magnetic adsorbent that exhibits effective application in pharmaceutical wastewater treatment.
| S-EPMC7935931 | biostudies-literature
Project description:Defect sites exist abundantly in minerals and play a crucial role for a variety of important processes. Here molecular dynamics simulations are used to comprehensively investigate the adsorption behaviors, stabilities and mechanisms of metal ions on defective minerals, considering different ionic concentrations, defect sizes and contents. Outer-sphere adsorbed Pb(2+) ions predominate for all models (regular and defective), while inner-sphere Na(+) ions, which exist sporadically only at concentrated solutions for regular models, govern the adsorption for all defective models. Adsorption quantities and stabilities of metal ions on kaolinite are fundamentally promoted by defect sites, thus explaining the experimental observations. Defect sites improve the stabilities of both inner- and outer-sphere adsorption, and (quasi) inner-sphere Pb(2+) ions emerge only at defect sites that reinforce the interactions. Adsorption configurations are greatly altered by defect sites but respond weakly by changing defect sizes or contents. Both adsorption quantities and stabilities are enhanced by increasing defect sizes or contents, while ionic concentrations mainly affect adsorption quantities. We also find that adsorption of metal ions and anions can be promoted by each other and proceeds in a collaborative mechanism. Results thus obtained are beneficial to comprehend related processes for all types of minerals.
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Project description:Innovative kaolinite nanotubes (KNTs) are synthesized utilizing a simple technique involving a sonication-induced exfoliation process, followed by chemical scrolling reactions. The KNTs as a material have high reactivity and promising surface area to be used in the purification of water from cationic dyes (safranin (SF) and malachite green (MG)) and anionic dyes (methyl orange (MO) and Congo red (CR)). The kinetic studies of the four dyes SF, MG, CR, and MO show an equilibration time interval of 240 min. The SF, MG, CR, and MO dyes' uptake reactions are in agreement with the kinetic behavior of the pseudo-first-order model and the equilibrium properties of the Langmuir model. Such modeling results, in addition to the Gaussian energies from the Dubinin-Radushkevich (D-R) model (SF (1.01 kJ/mol), MG (1.08 kJ/mol), CR (1.11 kJ/mol), and MO (1.65 kJ/mol)), hypothesize monolayer adsorption of the four dyes by physical reactions. The KNTs show theoretical q max values of 431.6, 489.9, 626.2, and 675.5 (mg/g) for SF, MG, CR, and MO, respectively. The thermodynamic examination of SF, MG, CR, and MO adsorption reactions using KNTs verifies their adsorption by exothermic and spontaneous reactions. The KNT adsorbents achieve promising adsorption results in the presence of different coexisting ions and show significant recyclability properties. Therefore, the production of KNTs from kaolinite shows a strong effect on inducing the textural, physicochemical, and adsorption properties of clay layers as well as their affinity for different species of synthetic dyes.
| S-EPMC7808155 | biostudies-literature
Project description:Effects of pH on adsorption and removal efficiency of ionizable organic compounds (IOCs) by environmental adsorbents are an area of debate, because of its dual mediation towards adsorbents and adsorbate. Here, we probe the pH-dependent adsorption of ionizable antibiotic oxytetracycline (comprising OTCH2 (+), OTCH(±), OTC(-), and OTC(2-)) onto cyclodextrin polymers (CDPs) with the nature of molecular recognition and pH inertness. OTCH(±) commonly has high adsorption affinity, OTC(-) exhibits moderate affinity, and the other two species have negligible affinity. These species are evidenced to selectively interact with structural units (e.g., CD cavity, pore channel, and network) of the polymers and thus immobilized onto the adsorbents to different extents. The differences in adsorption affinity and mechanisms of the species account for the pH-dependent adsorption of OTC. The mathematical equations are derived from the multiple linear regression (MLR) analysis of quantitatively relating adsorption affinity of OTC at varying pH to adsorbent properties. A combination of the MLR analysis for OTC and molecular recognition of adsorption of the species illustrates the nature of the pH-dependent adsorption of OTC. Based on this finding, ?-HP-CDP is chosen to adsorb and remove OTC at pH 5.0 and 7.0, showing high removal efficiency and strong resistance to the interference of coexisting components.
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Project description:A metal-organic framework, Zn-[2-methylimidazolate] frameworks (ZIF-8), was used as adsorbent material to remove different concentrations of oxytetracycline (OTC) antibiotic in a fixed-bed column. The OTC was studied at concentrations of 10, 25 and 40 mg L(-1). At 40 mg L(-1), the breakthrough point was reached after approximately 10 minutes, while at 10 and 25 mg L(-1) this point was reached in about 30 minutes. The highest removal rate of 60% for the 10 mg L(-1) concentration was reached after 200 minutes. The highest adsorption capacity (28.3 mg g(-1)) was attained for 25 mg L(-1) of OTC. After the adsorption process, a band shift was observed in the UV-Vis spectrum of the eluate. Additional studies were carried out to determine the cause of this band shift, involving a mass spectrometry (MS) analysis of the supernatant liquid during the process. This investigation revealed that the main route of adsorption consisted of the coordination of OTC with the metallic zinc centers of ZIF-8. The materials were characterized by thermal analysis (TA), scanning electron microscopy (SEM), powder X-ray diffraction (XRD), and infrared spectroscopy (IR) before and after adsorption, confirming the presence of OTC in the ZIF-8 and the latter's structural stability after the adsorption process.
| S-EPMC4461271 | biostudies-literature
Project description:Computational models of clay minerals and their interactions with the surrounding medium are highly valuable to study adsorption processes at an atomistic resolution, which may be relevant in different areas such as chromatography, environmental chemistry, and so forth. In this work, we analyzed the effect of the treatment of long-range interactions on the polarization of kaolinite-water interfacial systems in terms of structural, electric and dynamic properties, and hydrogen bonds. When using conventional three-dimensional (3D) Ewald summation, water molecules were more structured on the alumina interface of the kaolinite compared to simulations, in which the periodicity perpendicular to the plane was effectively removed. By applying an external electric field to the latter simulations, we were able to reproduce results obtained with the 3D Ewald summation. We proved that the induced polarization promotes adsorption processes of polar and charged species from aqueous solutions using a glyphosate molecule (widely used herbicide) as a particular example. The polarization phenomena raised from the simulation setup should be accounted for carefully in simulations of adsorption processes, which involve periodic images of polar interfaces. An inappropriate treatment of long-range electrostatic interactions can easily lead to artifacts and/or erroneous results.
| S-EPMC7610636 | biostudies-literature
Project description:From a genetic standpoint, Streptomyces rimosus is arguably the best-characterized industrial streptomycete as the producer of oxytetracycline and other tetracycline antibiotics. Although resistance to these antibiotics has reduced their clinical use in recent years, tetracyclines have an increasing role in the treatment of emerging infections and noninfective diseases. Procedures for in vivo and in vitro genetic manipulations in S. rimosus have been developed since the 1950s and applied to study the genetic instability of S. rimosus strains and for the molecular cloning and characterization of genes involved in oxytetracycline biosynthesis. Recent advances in the methodology of genome sequencing bring the realistic prospect of obtaining the genome sequence of S. rimosus in the near term.
| S-EPMC1594589 | biostudies-literature