scholarly journals Hybrid Porous Microparticles Based on a Single Organosilica Cyclophosphazene Precursor

2020 ◽  
Vol 21 (22) ◽  
pp. 8552
Author(s):  
Vanessa Poscher ◽  
George S. Pappas ◽  
Oliver Brüggemann ◽  
Ian Teasdale ◽  
Yolanda Salinas

Porous organosilica microparticles consisting of silane-derived cyclophosphazene bridges were synthesized by a surfactant-mediated sol-gel process. Starting from the substitution of hexachlorocyclotriphosphazene with allylamine, two different precursors were obtained by anchoring three or six alkoxysilane units, via a thiol-ene photoaddition reaction. In both cases, spherical, microparticles (size average of ca. 1000 nm) with large pores were obtained, confirmed by both, scanning and transmission electron microscopy. Particles synthesized using the partially functionalized precursor containing free vinyl groups were further functionalized with a thiol-containing molecule. While most other reported mesoporous organosilica particles are essentially hybrids with tetraethyl orthosilicate (TEOS), a unique feature of these particles is that structural control is achieved by exclusively using organosilane precursors. This allows an increase in the proportion of the co-components and could springboard these novel phosphorus-containing organosilica microparticles for different areas of technology.

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1128 ◽  
Author(s):  
Nguyen-Phuong-Dung Tran ◽  
Ming-Chien Yang

In this study, silicone nanoparticles (SiNPs) were prepared from polydimethylsiloxane (PDMS) and tetraethyl orthosilicate (TEOS) via the sol-gel process. The resultant SiNPs were characterized by dynamic light scattering (DLS), transmission electron microscope (TEM), and scanning electron microscope (SEM). These SiNPs were then blended with 2-hydroxyethylmethacrylate (HEMA) and 1-vinyl-2-pyrrolidinone (NVP) before polymerizing into hydrogel contact lenses. All hydrogels were subject to characterization, including equilibrium water content (EWC), contact angle, and oxygen permeability (Dk). The average diameter of SiNPs was 330 nm. The results indicated that, with the increase of SiNPs content, the oxygen permeability increased, while the EWC was affected insignificantly. The maximum oxygen permeability attained was 71 barrer for HEMA-NVP lens containing 1.2 wt% of SiNPs with an EWC of 73%. These results demonstrate that by loading a small amount of SiNPs, the Dk of conventional hydrogel lenses can be improved greatly. This approach would be a new method to produce oxygen-permeable contact lenses.


2020 ◽  
Vol 10 (17) ◽  
pp. 5960
Author(s):  
Suheir Omar ◽  
Raed Abu-Reziq

We describe, for the first time, a successful strategy for synthesizing chiral periodic mesoporous organosilica nanoparticles (PMO NPs). The chiral PMO nanoparticles were synthesized in a sol–gel process under mild conditions; their preparation was mediated by hydrolysis and condensation of chiral-bridged organo-alkoxysilane precursor compounds, (OR‘)3Si-R-Si(OR‘)3, in the presence of cetyltrimethylammonium bromide (CTAB) surfactant. The resulting nanoparticles were composed merely from a chiral- bridged organo-alkoxysilane monomer. These systems were prepared by applying different surfactants and ligands that finally afforded monodispersed chiral PMO NPs consisting of 100% bridged-organosilane precursor. In addition, the major advancement that was achieved here was, for the first time, success in preparing magnetic chiral PMO NPs. These nanoparticles were synthesized by the co-polymerization of 1,1′-((1R,2R)-1,2-diphenylethane-1,2-diyl)bis(3-(3-(triethoxysilyl) propyl) urea) chiral monomer by an oil in water (o/w) emulsion process, to afford magnetic chiral PMO NPs with magnetite NPs in their cores. The obtained materials were characterized with high-resolution scanning electron microscopy (HR-SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray (EDX) spectroscopy, powder X-ray diffraction (XRD), solid-state NMR analysis, circular dichroism (CD) analysis, and nitrogen sorption analysis (N2-BET).


2013 ◽  
Vol 284-287 ◽  
pp. 230-234
Author(s):  
Yu Jen Chou ◽  
Chi Jen Shih ◽  
Shao Ju Shih

Recent years mesoporous bioactive glasses (MBGs) have become important biomaterials because of their high surface area and the superior bioactivity. Various studies have reported that when MBGs implanted in a human body, hydroxyl apatite layers, constituting the main inorganic components of human bones, will form on the MBG surfaces to increase the bioactivity. Therefore, MBGs have been widely applied in the fields of tissue regeneration and drug delivery. The sol-gel process has replaced the conventional glasses process for MBG synthesis because of the advantages of low contamination, chemical flexibility and lower calcination temperature. In the sol-gel process, several types of surfactants were mixed with MBG precursor solutions to generate micelle structures. Afterwards, these micelles decompose to form porous structures after calcination. Although calcination is significant for contamination, crystalline and surface area in MBG, to the best of the authors’ knowledge, only few systematic studies related to calcination were reported. This study correlated the calcination parameters and the microstructure of MBGs. Microstructure evaluation was characterized by transmission electron microscopy and nitrogen adsorption/desorption. The experimental results show that the surface area and the pore size of MBGs decreased with the increasing of the calcination temperature, and decreased dramatically at 800°C due to the formation of crystalline phases.


2015 ◽  
Vol 47 (1) ◽  
pp. 1-12 ◽  
Author(s):  
M. Mazúr ◽  
L. Husáriková ◽  
M. Valko ◽  
C. J. Rhodes

2010 ◽  
Vol 113-116 ◽  
pp. 2266-2270
Author(s):  
Jing Li ◽  
Wei Xue ◽  
Yong Zhao ◽  
Zhi Miao Wang

A novel method of microemulsion coupling with sol–gel process was used for preparation of porous silica using tetraethyl orthosilicate as silicon source. Effect of solvent and catalyst on the surface texture properties was investigated respectively. The results showed that porous silica with large specific surface area (738.65 m2/g) and high pore volume (2.01 cm3/g) was obtained. However, the mesopores in silica were arranged in disorder and showed great ununiformity in shape and arrangement. To obtain porous silica with desired texture properties, an appropriate dosage of ethanol and higher HCl concentration were needed.


2014 ◽  
Vol 543-547 ◽  
pp. 3741-3744
Author(s):  
Quan Jing Mei ◽  
Cong Ying Li ◽  
Jing Dong Guo ◽  
Gui Wang ◽  
Hai Tao Wu

The ecandrewsite-type ZnTiO3was successfully synthesized by the aqueous sol-gel method using TiO2dioxide and zinc nitrate as starting materials instead of expensive organic solvent and metal alkoxides. The as-prepared nanopowders were characterized by X-ray diffraction (XRD), differential thermal analysis (DTA) and transmission electron microscopy (TEM), respectively. The results showed that the calcination process of gel consisted of a series of oxidation and combustion reactions, accompanied by significantly exothermal effects. Highly reactive nanosized ZnTiO3powders were successfully obtained at 850 °C with particle size ~50 nm. By comparison, the aqueous sol-gel process was the most effective and least expensive technique used for the preparation of ZnTiO3nanopowders.


2007 ◽  
Vol 1007 ◽  
Author(s):  
Sorin Ivanovici ◽  
Christoph Rill ◽  
Claudia Feldgitscher ◽  
Guido Kickelbick

ABSTRACTHybrid materials based on polysiloxanes and metal oxides (SiO2, TiO2, ZrO2) were prepared by hydrosilation of allyl acetoacetate (AAA) modified metal alkoxides (M(OR)4; M = Ti, Zr; R = ethyl, isopropyl) or vinyl triethoxysilane with poly(dimethylsiloxane-co-hydrosiloxane) (PDMS-co-PMHS). The obtained compounds acted as single-source precursors in the sol-gel process. Various spectroscopic methods showed the complete functionalization of the polysiloxane chains with the complexes. When alcohols were used as solvents in the sol-gel process, hybrid nanoparticles were obtained, as observed by dynamic light scattering (DLS) measurements, transmission electron microscopy (TEM), and spectroscopic methods such as NMR and FT-IR.


2019 ◽  
Vol 280 ◽  
pp. 03010 ◽  
Author(s):  
Dwi Rasy Mujiyanti ◽  
Muthia Elma ◽  
Mufidah Amalia

Interlayer-free glucose carbonized template silica membranesbased on tetraethyl orthosilicate (TEOS) and glucose were successfullyprepared using an acid-base catalysed sol-gel method for artificial brinewater desalination (7.5% wt NaCl solution %) at temperatures range from25, 40 and 60 °C. These membranes calcined at 250 and 400 °C. Themembranes were fabricated through sol-gel process by using TEOS(tetraethyl orthosilicate); ethanol; nitric acid; ammonia; aquadest andglucose as a template. By molar ratio is 1: 38: 0.0007: 0.0003: 5 and0.25%; 0.5%, 1% w/v glucose as template. The results show the highestwater fluxes of 1.8, 2.2 and 4.8 kg m−2 h−1 for 25, 40 and 60 °Cdesalination process with excellent salt rejections of 99.5, 99.5 and 99.7%, respectively. It was found that the higher the NaCl solution temperature asfeed solution as well as glucose concentration (0.25% to 1% wt) astemplate attached in the silica matrixes, the higher water fluxes eventhough the salt rejection remain the same. This study demonstrates that theorganosilica membranes offered the carbonized silica mesostructuremembranes with excellent separation of water from the hydrated salt ions, particularly for processing brine salt solutions.


2019 ◽  
Vol 113 (1) ◽  
pp. 511-517
Author(s):  
Masumeh Ziaee ◽  
Asgar Babamir-Satehi

Abstract Nanostructured silica can be used as a carrier of pesticides to enhance stability and controlled release of agrochemicals with an effective concentration on target pests. Silica nanoparticles (SNPs) were synthesized by sol–gel process and employed as a carrier of three different insecticides including deltamethrin, pyriproxyfen, and chlorpyrifos. The SNPs were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis and the insecticides-loaded in SNPs were characterized by transmission electron microscopy (TEM). The toxicity of insecticides alone and loaded in SNPs was evaluated against small and large larvae of Trogoderma granarium Everts on concrete surfaces. The immediate mortality was counted after 1, 3, and 7 d of exposure, and then surviving individuals were transferred to untreated surfaces for seven more days, with delayed mortality was recorded. Small larvae were more susceptible than large ones on all insecticide treatments. In addition, insecticides loaded in silica nanoparticles were more effective when compared with application of the insecticides alone. For immediate mortality, deltamethrin loaded in SNPs was the most efficient treatment causing 70.5% mortality on small and 55.5% mortality on large larvae after 7 d of exposure to the highest concentration. Pyriproxyfen loaded in SNPs caused low immediate mortality, but the mortality increased in delayed count indicated that the insecticide could control the larvae even after they have been removed from treated surfaces. It can be concluded that loading insecticides in SNPs could significantly increase their insecticidal efficiency, but this increase was compound-dependent.


2011 ◽  
Vol 399-401 ◽  
pp. 390-393
Author(s):  
Ai Huan Gao ◽  
Pi Hui Pi ◽  
Jiang Cheng ◽  
Zhuo Ru Yang

Aluminum sheet was encapsulated by inorganic-organic hybrid film through a base catalyzed sol-gel method using organic acrylate silane resin PMBV and TEOS as precursors. FTIR and AFM characterizations prove that PMBV and TEOS have hydrolyzed and co-condensed with each other in the sol-gel process to form an uniform film on the surface of aluminum sheet. XPS result shows hydroxyl groups on aluminum surface have taken part in the co-condensation reaction.


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