2003
DOI: 10.1016/s0022-3093(03)00007-3
|View full text |Cite
|
Sign up to set email alerts
|

Comparative study of the sol–gel processes starting with different substituted Si-alkoxides

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

2
46
0

Year Published

2007
2007
2016
2016

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 78 publications
(48 citation statements)
references
References 30 publications
2
46
0
Order By: Relevance
“…The NMR spectrum of the pure MTEOS precursor (Fig. 1) shows a single T 0 0 peak located at −44.03 ppm confirming the absence of any hydrolysed or modified regions respectively [15]. These bands are actually composed of several peaks indicating different degrees of hydrolysis for the silicon atom in each configuration, as summarised in Table 1.…”
Section: Resultsmentioning
confidence: 86%
See 1 more Smart Citation
“…The NMR spectrum of the pure MTEOS precursor (Fig. 1) shows a single T 0 0 peak located at −44.03 ppm confirming the absence of any hydrolysed or modified regions respectively [15]. These bands are actually composed of several peaks indicating different degrees of hydrolysis for the silicon atom in each configuration, as summarised in Table 1.…”
Section: Resultsmentioning
confidence: 86%
“…At the higher temperature the sol-gel dried faster than at the lower temperature and a thermal treatment of the gels at 50-70 • C was high enough to allow the evaporation of water, organic solvents and other moisture contents. Crucially this temperature range is below the softening (deformation) temperature of the polypropylene microtitre plates and, therefore, was chosen Table 1 Assignments of 29 Si NMR signals for monomeric and oligomeric species obtained from the metal doped MTEOS sol-gel [15]. as the curing temperature of the sol-gel.…”
Section: Thermal Analysismentioning
confidence: 99%
“…In HCl-catalysed reactions, hydrolysis is faster than condensation (Devreux et al 1990;Meixner and Dyer 1999), and alkyl-substituted trialkoxysilanes hydrolyse faster than the corresponding tetraalkoxysilanes (Himmel et al 1990). In particular, MTEOS hydrolyses faster than the TEOS monomer during each sequential hydrolysis reaction (Fyfe and Aroca 1997;Jitianu et al 2003). The replacement of the acidic conditions of an alkoxy by non-hydrolysable radicals leads to higher hydrolysis rates because the inductive effect of these radicals lowers the positive charge on the silicon and increases the negative charge on the oxygen atoms around the silicon atom as compared with TEOS (Devreux et al 1990;Jitianu et al 2003).…”
Section: Resultsmentioning
confidence: 99%
“…In particular, MTEOS hydrolyses faster than the TEOS monomer during each sequential hydrolysis reaction (Fyfe and Aroca 1997;Jitianu et al 2003). The replacement of the acidic conditions of an alkoxy by non-hydrolysable radicals leads to higher hydrolysis rates because the inductive effect of these radicals lowers the positive charge on the silicon and increases the negative charge on the oxygen atoms around the silicon atom as compared with TEOS (Devreux et al 1990;Jitianu et al 2003). Due to the fast hydrolysis rate, the formation of siloxane bonds controls the condensation rate, which in acidic media increases as a logarithm of time.…”
Section: Resultsmentioning
confidence: 99%
“…The amount, position and intensity of the bands from organics, when resolved in reference to literature data, seems to be evidently connected with organic additives have been employed [9,13,14]. Bands at around 562-576 cm -1 from absorption of lithium in LiClO 4 and bonded to organics, are observed in the FTIR spectra of all the hybrid electrolytes obtained.…”
Section: Samplementioning
confidence: 62%