4.1. Synthesis of Mesoporous Silica Nanoparticles (MCM-41 Generation)

MS Muhammad Hamid Siddique
SB Sidra Bukhari
IK Inam Ullah Khan
AE Asiya Essa
ZA Zain Ali
US Usama Sabir
OA Omiya Ayoub
HS Haleema Saadia
MY Muhammad Yaseen
AS Aneesa Sultan
IM Iram Murtaza
PK Philip G. Kerr
MB Mashooq Ahmad Bhat
MA Mariam Anees
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Mesoporous silica nanoparticles were synthesized using a chemical method [41]. The pH of deionized water (442 mL) was kept at 11 by adding 29% ammonium hydroxide (Sigma-Aldrich Cat. No. 1336-21-6; EMSURE®, Darmstadt, Germany) dropwise. The solution was heated to 50 °C, and 0.279 g of cetyltrimethylammonium bromide (CTAB) (Sigma-Aldrich Cat No. 57-09-0; Calbiochem®, Darmstadt, Germany) was added while stirring continuously. The pH was maintained at 10.3, and the solution was allowed to cool to room temperature. Next, tetramethyl orthosilicate (TMOS, 1.394 mL) (Sigma-Aldrich Cat. No. 78-10-4; Darmstadt, Germany) was added with constant stirring, resulting in turbidity after 2 min. The solution was left to stir overnight, followed by filtration and washing with deionized water. The obtained particles were dried at 90 °C and calcined at 500 °C for 5 h, yielding a white product. The product was finely ground into powder form. The dried powder was refluxed in methanol (100 mL) (Sigma-Aldrich Cat No. 67-56-1; Darmstadt, Germany) with concentrated HCl (1 mL) (Sigma-Aldrich Cat No. 7647-01-0; Darmstadt, Germany) for 24 h at 50 °C to remove the CTAB template. The resulting mesoporous silica nanoparticles (MSN) were isolated by filtration, extensively washed with water and methanol, and then dried at 100 °C for 24 h.

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