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Showing 2 results for Silane

S. M. Alduwaib, Muhannad M. Abd, Israa Mudher Hassan,
Volume 19, Issue 3 (9-2022)
Abstract

Background: Superhydrophobic materials which have contact angle higher than 150°, considering their widespread applications, are very important for researchers.
Method: In this research, silica nanopowder was synthesized successfully using inexpensive sodium silicate source and very simple and facile method. Synthesis of hydrophobic solution was carried out by sol-gel method. The surface modification of silica nanopowder was performed using different silane/siloxane polymers and was deposited on glass slides. For characterization of the samples XRD, FESEM, EDX, TEM, FTIR, and Raman analysis were used.
Results: The XRD result shows a very wide peak at 2q = 24.7° which indicates the amorphous nature of the silica particles. The results of the performed characteristics confirm the synthesis of silica nanopowder with the size of less than 25 nm. The EDX spectrum shows that only Si and O elements are present in the structure and no impurities are visible. The contact angle between water droplet and thin films was measured and the effect of different synthesis parameters on the contact angle was studied. Among the studied polymers and solvents, the most hydrophobicity was obtained using TMCS polymer and xylene solvent. The optimized sample has a maximum contact angle of 150.8°.
Conclusion: The synthesized thin films have superhydrophobic properties and the method used in this research can be developed for use in industrial applications.
Ali Hasanzade Salmasi, Mahban Zarei, Shadab Safarzadeh Khosroshahi, Soolmaz Heidari, Farhood Najafi, Mojtaba Ghomayshi, Katayoun Lesani,
Volume 20, Issue 3 (9-2023)
Abstract

Amorphous calcium phosphate (ACP) which is a transient phase in natural bio-mineralization process has recently gained the spotlight. This study aimed to assess the effect of incorporation of nano-ACP (NACP) in a dental adhesive with/without surface treatment with silane coupling agent on bond strength. NACP was synthesized by the wet chemical precipitation technique. To characterize the structure of NACP, X-ray diffraction, scanning electron microscopy and energy dispersive X-ray spectroscopy were used. Forty molars were randomized into 4 groups of 10. The teeth were restored with composite resin and the bonding agent (one of the four groups). Adper Single Bond 2 was used as the control group. In 4wt% NACP group, NACP fillers were added to the bonding agent. In 0.4wt% and 4wt% SNACP groups, silanized NACP fillers were added to the bonding agent. Finally, the mode of failure of specimens was determined. Data were analyzed by one-way ANOVA and Tukey's post-hoc tests. P<0.05 was considered statistically significant. Addition of 4wt% non-silanized NACP decreased the bond strength compared with the control group (P<0.05). The bond strength of the groups with silanized fillers was not significantly different from that of the control group. Addition of silanized NACP to dental adhesive had no significant adverse effect on bond strength, which is a promising finding to pave the way for the synthesis of bonding agents containing bioactive fillers.

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