Hollow Microspheres of Porous Silica Prepared Starting from a Hybrid Containing Chitosan

2000 ◽  
Vol 628 ◽  
Author(s):  
Pedro J. Retuert ◽  
Raul Quijada ◽  
Catalina Lafourcade

ABSTRACTThe combination of sols containing silica polymers, prepared by the sol-gel method under conditions of nearly linear chain growth, with solutions of the biopolymer chitosan has allowed us to obtain hybrid materials in the form of films or particles. In these hybrid nanocomposites, the organic and inorganic phases are associated through hydrogen bonds. In this work we present the preparation of hybrid xerogels of spherical morphology and their transformation into hollow spherical particles of silica with high specific area (276 m2/g) and a pore volume of 0.23 cm3/g. The xerogel particles were obtained by precipitation and subsequent drying. Thereafter, chitosan was extracted partially with acetic acid (5%) and finally the product was calcined at 550°C for two hours. The SEM micrograph shows that the silica particles were obtained as hollow spheres with size in the range between 10 and 100 μm. By using larger magnification, it was found that much smaller spheres of about 0.01 μm constitute the surface of these hollow spheres. Porosimetry shows the presence of micropores as well as mesopores. The observed morphology is discussed on the basis of a coprecipitation process conditioned by an association of both organic and inorganic phases in the precursor hybrid sol.

2003 ◽  
Vol 18 (2) ◽  
pp. 487-494 ◽  
Author(s):  
J. Retuert ◽  
R. Quijada ◽  
V. Arias ◽  
M. Yazdani-Pedram

In this paper, we report the preparation by the sol-gel technique of organic–inorganic hybrid composites containing the biopolymer chitosan incorporated in a siloxane-based inorganic network. The hybrid xerogels were transformed into porous silica particles by elimination of the organic phase. Surface characteristics of the silica samples can be easily tailored. In this way Brunauer–Emmett–Teller areas, pore volume, and pore diameter of the prepared silica can be predetermined within a wide range. Morphology of the particles at longer length scales can be designed to obtain either irregularly shaped particles with layered morphology or spherical particles. The results are explained on the basis of the cationic polyelectrolytic properties of chitosan, which allows easy association with siloxane oligomers, the precursors of silica in forming hybrid nanocomposites.


Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 963
Author(s):  
Ekaterina S. Dolinina ◽  
Elena V. Parfenyuk

Powerful antioxidant α-lipoic acid (LA) exhibits limited therapeutic efficiency due to its pharmacokinetic properties. Therefore, the purpose of this work was to evaluate the ability of silica-based composites of LA as well as its amide (lipoamide, LM), as new oral drug formulations, to control their release and maintain their therapeutic concentration and antioxidant activity in the body over a long time. The composites synthesized at different sol–gel synthesis pH and based on silica matrixes with various surface chemistry were investigated. The release behavior of the composites in media mimicking pH of digestive fluids (pH 1.6, 6.8, and 7.4) was revealed. The effects of chemical structure of the antioxidants, synthesis pH, surface chemistry of the silica matrixes in the composites as well as the pH of release medium on kinetic parameters of the drug release and mechanisms of the process were discussed. The comparative analysis of the obtained data allowed the determination of the most promising composites. Using these composites, modeling of the release process of the antioxidants in accordance with transit conditions of the drugs in stomach, proximal, and distal parts of small intestine and colon was carried out. The composites exhibited the release close to the zero order kinetics and maintained the therapeutic concentration of the drugs and antioxidant effect in all parts of the intestine for up to 24 h. The obtained results showed that encapsulation of LA and LM in the silica matrixes is a promising way to improve their bioavailability and antioxidant activity.


2019 ◽  
Vol 234 (10) ◽  
pp. 647-655
Author(s):  
Zohra Nazir Kayani ◽  
Atiqa Aslam ◽  
Rabia Ishaque ◽  
Syeda Nosheen Zahra ◽  
Hifza Hanif ◽  
...  

Abstract Nickel oxide thin films have been prepared by sol-gel dip-coating technique on glass substrate. It is shown that nickel oxide thin films have poly crystalline nature. Nickel oxide thin films exhibit high transmission (39–85%) in the wavelength range of 400–900 nm, strong absorption between 300 and 400 nm wavelengths and decrease of band gap values are in the range 3.69–3.27 eV with increase of withdrawal speed. High band gap at low withdrawal speed is because of the small average crystallite size, which decreases with increase in withdrawal speed. The SEM micrograph shows cubic crystallites and surface of thin films become dense, smooth and homogeneous with an increase in withdrawal speed. Assessment of nickel oxide deposition conditions provides gateway for effective and cheap solar cells.


Metals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 463
Author(s):  
Srecko Stopic ◽  
Felix Wenz ◽  
Tatjana-Volkov Husovic ◽  
Bernd Friedrich

Silica has sparked strong interest in hydrometallurgy, catalysis, the cement industry, and paper coating. The synthesis of silica particles was performed at 900 °C using the ultrasonic spray pyrolysis (USP) method. Ideally, spherical particles are obtained in one horizontal reactor from an aerosol. The controlled synthesis of submicron particles of silica was reached by changing the concentration of precursor solution. The experimentally obtained particles were compared with theoretically calculated values of silica particles. The characterization was performed using a scanning electron microscope (SEM) and energy-dispersive X-ray spectroscopy (EDS). X-ray diffraction, frequently abbreviated as XRD, was used to analyze the structure of obtained materials. The obtained silica by ultrasonic spray pyrolysis had an amorphous structure. In comparison to other methods such as sol–gel, acidic treatment, thermal decomposition, stirred bead milling, and high-pressure carbonation, the advantage of the ultrasonic spray method for preparation of nanosized silica controlled morphology is the simplicity of setting up individual process segments and changing their configuration, one-step continuous synthesis, and the possibility of synthesizing nanoparticles from various precursors.


1998 ◽  
Vol 519 ◽  
Author(s):  
L. Bergogne ◽  
S. Fennouh ◽  
J. Livage ◽  
C. Roux

AbstractBioencapsulation in sol-gel materials has been widely studied during the past decade. Trapped species appear to retain their bioactivity in the porous silica matrix. Small analytes can diffuse through the pores allowing bioreactions to be performed in-situ, inside the sol-gel glass. A wide range of biomolecules and micro-organisms have been encapsulated. The catalytic activity of enzymes is used for the realization of biosensors or bioreactors. Antibody-antigen recognition has been shown to be feasible within sol-gel matrices. Trapped antibodies bind specifically the corresponding haptens and can be used for the detection of traces of chemicals. Even whole cells are now encapsulated without any alteration of their cellular organization. They can be used for the production of chemicals or as antigens for immunoassays.


2000 ◽  
Vol 612 ◽  
Author(s):  
Sylvie Acosta ◽  
André Ayral ◽  
Christian Guizard ◽  
Charles Lecornec ◽  
Gérard Passemard ◽  
...  

AbstractPorous silica exhibits attractive dielectric properties, which make it a potential candidate for use as insulator into interconnect structures. A new way of preparation of highly porous silica layers by the sol-gel route was investigated and is presented. The synthesis strategy was based on the use of common and low toxicity reagents and on the development of a simple process without gaseous ammonia post-treatment or supercritical drying step. Defect free layers were deposited by spin coating on 200 mm silicon wafers and characterized. Thin layers with a total porosity larger than 70% and an average pore size of 5 nm were produced. The dielectric constant measured under nitrogen flow on these highly porous layers is equal to ∼ 2.5, which can be compared to the value calculated from the measured porosity, ∼ 1.9. This difference is explained by the presence of water adsorbed on the hydrophilic surface of the unmodified silica.


2021 ◽  
Vol 21 (10) ◽  
pp. 5143-5149
Author(s):  
Zhen Zhu ◽  
Wang-De Lin

This paper reports on a nanocomposite synthesized by sol–gel procedure comprising graphene sheets with hollow spheres of titanium dioxide (G/HS-TiO2) with varying weight percentages of graphene for the purpose of humidity sensors. The surface morphology of the nanocomposite was characterized using transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). The structural properties were examined using X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR). The response to 12–80% RH at room temperature exhibited sensitivity (S = 135). However, the relative humidity range of 12–90% at room temperature exhibited higher sensitivity (S = 557). Sensors fabricated using the proposed nanocomposite exhibited high sensitivity to humidity, high stability, rapid response times, and rapid recovery times with hysteresis error of less than 1.79%. These results demonstrate the outstanding potential of his material for the monitoring of atmospheric humidity. This study also sought to elucidate the mechanisms underlying humidity sensing performance.


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