Hybrid Silica Materials Applied for Fuchsine B Color Removal from Wastewaters.
Ontology highlight
ABSTRACT:
SUBMITTER: Fratilescu I
PROVIDER: S-EPMC8066414 | biostudies-literature |
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:The adsorptive performance of mesoporous silica-based materials towards inorganic (metal ions) and organic (dyes) water pollutants was investigated. Mesoporous silica materials with different particle size, surface area and pore volume were prepared and tailored with different functional groups. These materials were then characterised by solid-state techniques, namely vibrational spectroscopy, elemental analysis, scanning electron microscopy and nitrogen adsorption-desorption isotherms, allowing the successful preparation and structural modifications of the materials to be confirmed. The influence of the physicochemical properties of the adsorbents towards the removal of metal ions (Ni2+, Cu2+ and Fe3+) and organic dyes (methylene blue and methyl green) from aqueous solutions was also investigated. The results reveal that the exceptionally high surface area and suitable ζ-potential of the nanosized mesoporous silica nanoparticles (MSNPs) seem to favour the adsorptive capacity of the material for both types of water pollutants. Kinetic studies were performed for the adsorption of organic dyes by MSNPs and large-pore mesoporous silica (LPMS), suggesting that the process follows a pseudo-second-order model. The recyclability along consecutive adsorption cycles and the stability of the adsorbents after use were also investigated, showing that the material can be reused. Current results show the potentialities of novel silica-based material as a suitable adsorbent to remove pollutants from aquatic matrices with an applicability to reduce water pollution.
| S-EPMC10223029 | biostudies-literature
Project description:A mesoporous silica-based drug delivery device potentially useful for bone-specific drug delivery has been designed, developed and characterized starting from MSU-type mesoporous silica. The proposed system consists of a mesoporous silica nanoparticles (MSN) based vehicle, presenting alendronate as a targeting functionality for bone tissue while ibuprofen is used as a model molecule for the drugs to be delivered. The particles are functionalized on the external surface using a propionitrile derivative that is successively hydrolyzed to a carboxylic group. Alendronate, one of the most used member of the diphosphonate drug class, is electrostatically bonded to the external carboxyl functionalities of mesoporous silica. The obtained material has been characterized by powder X-ray diffraction, N2 adsorption-desorption porosimetry, UV-vis spectrophotometry, FT-IR spectrometry and MAS-NMR 13C and 29Si. Hydroxyapatite, which simulates the bone matrix, has been synthesized with the aim of testing the targeting activity of the obtained device. In a separate test, the MSNs have been loaded with ibuprofen, a non-steroidal anti-inflammatory drug (NSAID), and its release has been determined under neutral conditions by HPLC. Moreover, biological tests were carried out. The tested devices did not show any toxicity towards normal cells, confirming their high biocompatibility and the lack of off-target effects.
| S-EPMC9417532 | biostudies-literature
Project description:Highly porous carbon-silica composites (CSC) were prepared for the first time through a simple wet impregnation process and subsequent pyrolysis of low-value sugarcane by-products, namely molasses. These CSC materials demonstrate a distinct range of functionalities, which significantly differ from similar materials published in the literature. Importantly, the carbon-silica composites prepared at 800°C exhibited exceptional adsorption capacities for the azo-dye congo red (445 mg g-1), due to the graphitic carbon coating and unique functionality including C-O-C within the porous structure. Congo red adsorption capacity of the highly mesoporous graphitic carbon-silica composites significantly exceeds that of commercial activated carbon and silica, these carbon-silica composites therefore represent an effective step towards the development of porous bio-derived adsorbent for remediation of dye wastewaters. Both the porous properties (surface area and pore size distribution) and the functionality of the carbon coating were dependent on the temperature of preparation. The sustainable synthetic methods employed led to a versatile material that inherited the mesoporosity characteristics from the parent silica, demonstrating mesoporous volumes greater than 90% (as calculated from the total pore volume). Adsorption on the 800°C prepared carbon-silica composites demonstrated an excellent fit with the Langmuir isotherm and the pseudo-first-order kinetic model.
| S-EPMC7540760 | biostudies-literature
Project description:Gene expression profile analysis allowed to identify a panel of genes characteristic of silica materials effect on transformation process.
2022-06-01 | GSE133279 | GEO
Project description:Herein, it is reported how pseudomorphic transformation of divinylbenzene (DVB)-bridged organosilica@controlled pore glasses (CPG) offers the possibility to generate hierarchically porous organosilica/silica hybrid materials. CPG is utilized to provide granular shape/size and macroporosity and the macropores of the CPG is impregnated with organosilica phase, forming hybrid system. By subsequent pseudomorphic transformation, an ordered mesopore phase is generated while maintaining the granular shape and macroporosity of the CPG. Surface areas and mesopore sizes in the hierarchical structure are tunable by the choice of the surfactant and transformation time. Two-dimensional magic angle spinning (MAS) NMR spectroscopy demonstrated that micellar-templating affects both organosilica and silica phases and pseudomorphic transformation induces phase transition. A double-layer structure of separate organosilica and silica layers is established for the impregnated material, while a single monophase consisting of randomly distributed T and Q silicon species at the molecular level is identified for the pseudomorphic transformed materials.
| S-EPMC7497150 | biostudies-literature
Project description:One of the major obstacles to the reuse of recycled plastic materials is the emanation of after-process odors from recycled polymers and composites. Typically, recycled polymers are blended with an off-odor adsorbent additive in the recycling chain to eliminate these smells. This article describes an innovative ultrasonically assisted method of grafting poly(ethylene imine) (PEI) to silica nanoparticles (SiO2) initiated by benzoyl peroxide (BP) which acts as an odor remover. To prepare the PEI/Si, the branched PEI was grafted onto the silica surface without a coupling agent. This made the grafting process straightforward, easy and low in cost. Fourier Transform Infrared (FTIR) analysis confirmed the successful grafting of PEI to silica. The thermogravimetric analysis (TGA) indicated the formation of two different fractions: a polymeric fraction covalently attached to the nanoparticle surface and a non-grafted PEI fraction that was removed during extraction. Up to 30% of the grafted-PEI fractions were produced at the lowest BP concentration with the highest PEI molecular weight at silica-to-PEI weight ratios of (1:1) to (3:1). The sensory assessment showed a substantial reduction in overall odor intensity for 30% of the recycled plastic-containing materials and a ~75% reduction in volatile organic compounds (VOCs) for 100% of the recycled plastics. These results strongly suggest that this innovative PEI/Si nanocomposite can be successfully commercialized for odor removal. To the authors' best knowledge, this is the first reported work describing a one-pot reaction for grafting PEI to different nanoparticle surfaces.
| S-EPMC9268616 | biostudies-literature
Project description:One of the major goals in the materials science is the design and development of non-toxic, versatile, and efficient drug delivery systems. The study reported in this paper concerns the syntheses of poly(amidoamine) (PAMAM) dendrimers with tris(2-aminoethyl)amine as an amine core and different terminal amines, and their attachment to silica matrix. The obtained ethylenediamine (EDA), triethylenetetramine (TETA), tris(2-aminoethyl)amine (TREN) and 4,7,10-trioxa-1,13-tridecanediamine (TRI-OXA) dendrimers were introduced to the support surface via an epoxy linker, leading to a loading efficiency in the range of 0.054-0.113 mmol g-1, determined using elemental and thermogravimetric analyses. The materials exhibited high adsorption capacities towards the chosen model drugs: folic, salicylic and nicotinic acid. The investigated adsorption processes were found to follow the Freundlich isotherm model, with indication of the drugs' structure influence on the binding efficiency. Drug-loaded hybrid materials were also described for in vitro drug release in three pH-different paraphysiological media. The highest percentage release was obtained in the tests performed at pH 2.0, ranging between 35.42 and 99.83%. Satisfactory results and the versatility of PAMAM dendrimers may lead to the application of such materials not only as drug carriers dedicated to a wide range of pharmaceutics, but also as analytical tools for pre-concentration and/or the determination of biocompound contamination in samples.
| S-EPMC7321234 | biostudies-literature
Project description:Four kinds of soluble monomers, containing triarylamine (TAA) group with reactive siloxane group, were synthesized under mild conditions via the reaction between 3-(triethoxysilyl)propyl isocyanate (TEOSPIC) and four TAA derivatives, respectively. Then the corresponding colorless organic-inorganic hybrid materials (PSSOs) were derived from the hydrolytic condensation of the monomers. PSSOs revealed good solubility in polar solvents on account of the effect of propeller-like TAA unit as well as the auxo-action effect of the flexible chain within the monomers. The structural characteristics of these PSSOs were identified by 1H NMR, 29Si NMR, FT-IR spectroscopies and X-ray diffraction (XRD). The morphology, dynamic changes of the transmittance and current before and after electro-oxidizing reaction were studied, and didn't show significant change suggesting good stability of the PSSOs. Meanwhile, these PSSOs performed high contrast of optical transmittance change up to 84% with the highest coloration efficiency to 241 cm2·C-1. Furthermore, electrofluorescent properties of PSSOs were investigated with high-contrast.
| S-EPMC5677139 | biostudies-literature
Project description:The remarkable characteristics of graphene make it a model candidate for boosting the effectiveness of nano-adsorbents with high potential owing to its large surface area, π-π interaction, and accessible functional groups that interact with an adsorbate. However, the stacking of graphene reduces its influence adsorption characteristics and also its practical application. On the other hand, the widespread use of aromatic compounds in the industry has aggravated the contamination of the water environment, and how to effectively remove them has become a research hotspot. Herein, we develop the functionalization of silica nanoparticles on graphene oxide nanosheet (FGS) by a facile, cheap, and efficient synthesis protocol for adsorption of Trypan Blue (TB) and Bisphenol A (BPA). It was demonstrated that chemical activation with KOH at high autoclaving temperature successfully transformed rice husk ash (RHA) into FGS. The graphene oxide layered interlamination was kept open by using SiO2 to expose the interlayers' strong adsorption sites. XRD, EDX, FTIR, Raman spectroscopy, SEM, HR-TEM, and BET surface area are used to investigate the chemical composition, structure, morphology, and textural nature of the as-produced FGS hybrid nanocomposite. The various oxygen-containing functional groups of the hybrid nanocomposites resulted in a significantly increased adsorption capacity, according to experimental findings. In addition, FGS2, the best composite, has a specific surface area of 1768 m2g-1. Based on Langmuir isotherms, the maximal TB dye and BPA removal capacity attained after 30 min were 455 and 500 mg/g, respectively. The Langmuir isotherm model, a pseudo-second-order kinetic model, and an intraparticle diffusion model have all been used to provide mechanistic insights into the adsorption process. This suggests that BPA and TB adsorption on FGS2 is mostly chemically regulated monolayer adsorption. Due to its unique sp2-hybridized single-atom-layer structure, the exposed graphene oxide nanosheets' extremely hydrophobic effect, hydrogen bonding, and strong-electron donor-acceptor interaction contributed to their improved adsorption of BPA and TB. According to adsorption thermodynamics, FGS2 adsorption of TB and BPA is a spontaneous exothermic reaction that is aided by lowering the temperature. For adsorption-based wastewater cleanup, the produced nanocomposites with a regulated amount of carbon and silica in the form of graphene oxide and silica can be used. These findings suggest that functionalized GO/SiO2 hybrid nanocomposites could be a viable sorbent for the efficient and cost-effective removal of aromatic chemicals from wastewater.
| S-EPMC9054805 | biostudies-literature
Project description:This work is focused on a novel class of hybrid materials exhibiting enhanced optical properties and high surface areas that combine the morphology offered by the vinyl substituted silica host, and the excellent absorption and emission properties of 5,10,15,20-tetrakis(N-methyl-4-pyridyl)porphyrin-Zn(II) tetrachloride as a water soluble guest molecule. In order to optimize the synthesis procedure and the performance of the immobilized porphyrin, silica precursor mixtures of different compositions were used. To achieve the requirements regarding the hydrophobicity and the porous structure of the gels for the successful incorporation of porphyrin, the content of vinyltriacetoxysilane was systematically changed and thoroughly investigated. Substitution of the silica gels with organic groups is a viable way to provide new properties to the support. An exhaustive characterization of the synthesized silica samples was realised by complementary physicochemical methods, such as infrared spectroscopy (FT-IR), absorption spectroscopy (UV-Vis) and photoluminescence, nuclear magnetic resonance spectroscopy (29Si-MAS-NMR) transmission and scanning electron microscopy (TEM and SEM), nitrogen absorption (BET), contact angle (CA), small angle X ray and neutron scattering (SAXS and SANS). All hybrids showed an increase in emission intensity in the wide region from 575 to 725 nm (Q bands) in comparison with bare porphyrin. By simply tuning the vinyltriacetoxysilane content, the hydrophilic/hydrophobic profile of the hybrid materials was changed, while maintaining a high surface area. Good control of hydrophobicity is important to enhance properties such as dispersion, stability behaviour, and resistance to water, in order to achieve highly dispersible systems in water for biomedical applications.
| S-EPMC5951449 | biostudies-literature