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Triethoxysilane ethanol

Apart from Eu3+ and Tb3+, few studies have been reported on optical properties of lanthanide ions doped in ZnS nanociystals. Bol et al. (2002) attempted to incorporate Er3"1" in ZnS nanociystal by ion implantation. They annealed the sample at a temperature up to 800 °C to restore the crystal structure around Er3"1", but no Er3"1" luminescence was observed. Schmidt et al. (1998) employed a new synthesis strategy to incorporate up to 20 at% Er3"1" into ZnS (1.5-2 nm) cluster solutions which were stabilized by (aminopropyl)triethoxysilane (AMEO). Ethanolic AMEO-stabilized Er ZnS clusters in solutions fluoresce 200 times stronger at 1540 nm than that of ethanolic AMEO-Er complexes. This is explained by the very low phonon energies in ZnS QDs, and indicates that Er3+ ions are trapped inside chalcogenide clusters. However the exact position of Er3+ in ZnS clusters remains unknown. Further spectroscopic and structural analyses are required in order to obtain more detailed information. [Pg.142]

Divinylbenzene, styrene, a,a -azoisobutyronitrile and methacrylic monomers di(methacryloyloxymethyl)-naphthalene (DMN), methacrylic ester of p,p -dihydroxydiphenylpropane diglycidyl ether (MEDDE), and dimethacrylglycol-ethylene (DMGE) were received from Fluka and used without further purification. Polyfvinyl alcohol), /7-dccanol, ethanol, acetone and toluene (Merck), fumed silica with specific surface area of 300 m2/g (Kalush), triethoxysilane (Kremnepolimer) and hexamethyldisilazane (Fluka) were applied. [Pg.104]

Initial efforts to bond chitosan coatings to metal implant surfaces used ethanol/ water solutions, ranging from 95% ethanol and 5% water to 70% ethanol and 30% water, to deposit APTES onto the surface of titanium substrates [39, 46, 75, 78]. Ethanol and water have been used to deposit the silane because they are safe and easy to use. The use of ethanol/water to deposit APTES significantly increased the bond strength of chitosan on titanium from a mean 0.5 MPa for chitosan simply absorbed to the titanium to 1.5 MPa (Table 1) [46]. Using an isocyantopropyl-triethoxysilane (ICPTES), mechanical bond strengths were increased to between... [Pg.135]

Preparatitxi of photoinitiator modified silicas A certain amount (1 or 5 g) of the triethoxysilane photoinitiator (Id or le) was dissolved in 20 ml ethanol and 10 g silica gel was suspended in the solu-tisolid material was heated for 15 minutes at 150 °C under stirring. The photoinitiator modified silicas Ila-d were Wcished five times with 100 ml ethanol to remove adsorbed materials and dried overnight in vacuo. [Pg.107]

HMS have been chemically modified using (3-aminopropyl)triethoxysilane (APTES). A solution (30 ml) of HMS (0.1 g) and APTES (2 ml) was prepared in toluene. In fact, APTES, an aminosilane, can be used in the silanisation process to functionalise the HMS surfaces with alkoxysilane molecules. APTES can also be used to covalently bond thermoplastics to polydimethylsiloxane (PDMS). APTES-functionalised HMS surfaces have been shown to be non-toxic to embryonic rat cardiomyocytes in vitro. In this study, the resulting magnetite/silicon particles were washed with ethanol and then dried under vacuum at 60 C for 24 h [57]. The obtained amine-functionalised HMS (HMS-NHi) were dispersed by ultrasound in toluene (30 ml). Another modification involved D,L-lactide (0.4 g) and PEG (0.1 g), which were placed into a three-neck round-bottom flask containing a magnetic stirrer. The catalyst, Sn(Oct)2, was added to the flask at a concentration of 0.1% of the solution the flask was put into an oil bath to react for 24 h at 110 C in nitrogen under ambient conditions [58]. [Pg.135]

Triethoxysilane and a 1,0 M soln. of HgPtGlg in abs. isopropanol added drop-wise and simultaneously at 90-125° to pseudoionone, and heating continued 15 min. at 120-125° 2-(6,lO-dimethyl-2,5,9-undecatrienoxy) triethoxysilane (Y 78.5%) dissolved in ethanol containing coned. HGl, allowed to stand 17 hrs. at 18-20°, then the solvent distilled off in vacuo frans-geranylacetone (Y 77.8%). Also without isolation of the intermediate s. E. I. Kozlov, M. T. Yano-tovskii, and G. I. Samokhvalov, 34, 2748 (1964) G. A. 61, 14716d. [Pg.35]

We conducted experiments on the triethoxysilane SiH(OC2Hs)3 direct process by means of siUcon interaction with ethanol. Polymethylsiloxane fluids, vaseline oil, ethyl silicate (an oligoethoxysiloxane mixture of SiB+iO (OC2Hs)2( +2)), alkylbenzene, aloterm (alkyldiphenyl oxide) and termolan (alkylated naphthalene) were tested as a high-boiling solvent. [Pg.515]

AB) r piperazine (P), aniline (A), and 3-aminopropyl-triethoxysilane (AS). Glass slides were treated with amine at room temperature usually by immersing the slides for 5 min. in an amine-absolute ethanol solution. After removing the glass slides from the amine solution, the... [Pg.125]

TESPA- ([3-aminopropyl]triethoxysilane Sigma-Aldrich A3648) coated slides are prepared as follows. Wash slides in 10% HCl/70% ethanol, followed by 95%... [Pg.154]

Cleaned coverslips Wash in 70% ethanol/1% concentrated HCl and then 2% (TESPA) 3-aminopropyl- triethoxysilane/3-(triethoxysilyde)-propylamine for lOmin. Rinse in acetone for lOmin, then distilled water before drying. [Pg.748]

Turkel taub et al have described gas chromatographic methods for the determination of ethanol in triethoxysilane. They used a column containing 20% of silicone PFMS-3 supported on firebrick with hydrogen or helium as carrier gas and a katharometer detector. Turkel taub et al have also described a method for the determination of ethanol in triethoxysilane based on chromatography of 25°C on a 200 cm column containing 2% of petroleum jelly on fire brick (particle size 0.025 to 0.050 cm previously dried at 150 to 200°C). A flame ionization detector was used and hydrogen was employed as carrier gas (25 ml per minute). [Pg.234]

Fluoropropyl)triethoxysilane reacts with tris(2-hydroxyethyl)amine in the presence of ethanol and potassium hydroxide to form 1-3(fluoropropyl)silatrane [308]... [Pg.62]

Aminoethyl alcohol fi-Aminoethyl alcohol. See Ethanolamine 2-((2-Aminoethyl) amino) ethanol. See Aminoethylethanolamine N- HAminoeth ) minopropyl triethoxysilane... [Pg.1973]


See other pages where Triethoxysilane ethanol is mentioned: [Pg.111]    [Pg.118]    [Pg.461]    [Pg.334]    [Pg.494]    [Pg.105]    [Pg.640]    [Pg.115]    [Pg.968]    [Pg.26]    [Pg.295]    [Pg.968]    [Pg.115]    [Pg.408]    [Pg.414]    [Pg.176]    [Pg.32]    [Pg.218]    [Pg.92]    [Pg.92]    [Pg.334]    [Pg.226]    [Pg.278]    [Pg.478]    [Pg.1749]    [Pg.236]    [Pg.18]    [Pg.398]   
See also in sourсe #XX -- [ Pg.234 ]




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Triethoxysilane

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