Sol-Gel Synthesis and Preliminary Characterizations of Novel Silica Hybrid Xerogels

2014 ◽  
Vol 925 ◽  
pp. 354-358

Removed at authors request

2013 ◽  
Vol 594-595 ◽  
pp. 1009-1014
Author(s):  
S.A. Syed Nuzul Fadzli ◽  
S. Roslinda ◽  
Z. Firuz

Hybrid silica xerogel mesoporous composite was synthesized by a mild temperature acid catalysed sol-gel route where a natural copolymer; sodium alginate (Na-COOH) together with calcium oxide (CaO) powder were incorporated into silica sol precursor prior to gel formation. For this study, bulk xerogels samples were prepared with the amount of silica precursor and the natural copolymer was fixed meanwhile the loading of calcium oxide was varied at 10 and 20 wt%. The monolith silica was also synthesized as control parameter. The preliminary properties were investigated using XRD, FTIR and SEM together with EDS for elemental analysis. The calcium oxide powder used in this study was prepared from calcium hydroxide, CaOH compound, which was previously calcined at 1000°C for 3 hours in normal air. The component of calcium oxide and sodium alginate were found to be uniformly dispersed in matrixes without affecting the cross-linked silica formation. As the presence of the components in the silica matrixes, the synthesized hybrid xerogels were found to be crack-free, structurally amorphous and physically opaque. Furthermore, the hybrid xerogels samples were found to have denser bodies, smoother surface, and decreased in particle sizes and thus might produced less brittleness in nature compared to the monolith xerogels.


2010 ◽  
Vol 8 (4) ◽  
pp. 870-876 ◽  
Author(s):  
Georgi Chernev ◽  
Borislava Borisova ◽  
Lyudmila Kabaivanova ◽  
Isabel Salvado

AbstractThis work reports the sol-gel synthesis of silica hybrids. We determined the effect of the type and quantity of silica precursors and organic compounds on the resulting structure, surface area, nanostructure design and size, and potential applications. The structure of the synthesized hybrids was analyzed using FT-IR, XRD, BET-Analysis, SEM, and AFM. We demonstrate the immovilization of whole living thermophilic bacterial cells with cyanocompound degradation activity in the synthesized silica hybrid biomaterials by entrapment, chemical binding, and adsorption.


2008 ◽  
Vol 354 (2-9) ◽  
pp. 733-740 ◽  
Author(s):  
Bisserka Samuneva ◽  
Peter Djambaski ◽  
Elena Kashchieva ◽  
Georgi Chernev ◽  
Lyudmila Kabaivanova ◽  
...  

2021 ◽  
Vol 395 (1) ◽  
pp. 2000208
Author(s):  
Alessandra Fusco ◽  
Giovanna Donnarumma ◽  
Pina Caputo ◽  
Monica. Gallo ◽  
Michelina Catauro

2018 ◽  
Vol 133 (2) ◽  
pp. 1085-1092 ◽  
Author(s):  
Michelina Catauro ◽  
Daniele Naviglio ◽  
Roberta Risoluti ◽  
Stefano Vecchio Ciprioti

2008 ◽  
Vol 48 (1-2) ◽  
pp. 73-79 ◽  
Author(s):  
B. Samuneva ◽  
L. Kabaivanova ◽  
G. Chernev ◽  
P. Djambaski ◽  
E. Kashchieva ◽  
...  

2003 ◽  
Vol 780 ◽  
Author(s):  
R. Houbertz ◽  
J. Schulz ◽  
L. Fröhlich ◽  
G. Domann ◽  
M. Popall ◽  
...  

AbstractReal 3-D sub-νm lithography was performed with two-photon polymerization (2PP) using inorganic-organic hybrid polymer (ORMOCER®) resins. The hybrid polymers were synthesized by hydrolysis/polycondensation reactions (modified sol-gel synthesis) which allows one to tailor their material properties towards the respective applications, i.e., dielectrics, optics or passivation. Due to their photosensitive organic functionalities, ORMOCER®s can be patterned by conventional photo-lithography as well as by femtosecond laser pulses at 780 nm. This results in polymerized (solid) structures where the non-polymerized parts can be removed by conventional developers.ORMOCER® structures as small as 200 nm or even below were generated by 2PP of the resins using femtosecond laser pulses. It is demonstrated that ORMOCER®s have the potential to be used in components or devices built up by nm-scale structures such as, e.g., photonic crystals. Aspects of the materials in conjunction to the applied technology are discussed.


2019 ◽  
Vol 11 (3) ◽  
pp. 03021-1-03021-5
Author(s):  
V. S. Bushkova ◽  
◽  
I. P. Yaremiy ◽  
B. K. Ostafiychuk ◽  
N. I. Riznychuk ◽  
...  

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