Web of Science (Emerging Sources Citation Index)

Document Type: Original Research Article

Authors

1 Department of Chemistry, University of Zanjan, P.O. Box 45195-313, Zanjan, Iran

2 Department of Chemistry, University of Zanjan, P.O. Box 45195-313, Zanjan, Iran; Research Institute of Modern Biological Techniques (RIMBT), University of Zanjan, P.O. Box 45195-313, Zanjan

10.33945/SAMI/ECC.2020.8.4

Abstract

Silica nanoscale powders were obtained by heat treatment on the waste of laboratory silica gel HF254 available at the warehouse. That white solid was thermally treated at optimal conditions at 700 °C for 4 h and after decomposition of all of the materials, was refluxed with HCl (6 M) for 24 hours. Afterward, the prepared catalyst was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Brunauer–Emmett–Teller (BET) analysis. The average nanoparticle size was measured 25 nm. So the purpose was investigated on the attributes of the catalyst supported by chloro sulfuric acid and its application in the Fisher esterification reaction as an acid solid catalyst under solvent-free conditions. According to this, different parameters such as the types of alcohols and phenols and carbon chain length were studied by both nano-silica sulfuric acid (NSSA) and silica sulfuric acid (SSA) at the same conditions. In this case, the foundings illustrated esterification in the presence of NSSA was performed at reaction time less than SSA and the production yield of NSSA was higher than SSA. The obtained results in the mentioned method proved silica from the wastes of silica gel HF254 can be employed as a catalyst at the more reaction.

Graphical Abstract

Keywords

Main Subjects

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[32] S. Pathak, K.D. Ebnath, A. Pramanik, Beilstein J. Org. Chem., 2013, 9, 2344–2353.

[33] L. Wu1, X. Yang, F. Yan, Bull. Chem. Soc. Ethiop., 2011, 25, 151-155.

[34] D. Shobha, M. Adharvana Chari, K. Mukkanti, K.H. Ahn, J. Heterocyclic. Chem., 2009, 46, 1028-103.

 

[35] M. Thommes, K. Katsumi Kaneko, A.V. Neimark, J.P. Olivier, F. Rodriguez-Reinoso, J. Rouquerol, K.S.W. Sing, Pure Appl. Chem. 2015, 87, 1051–106.

[1]. L.S. Al Banna, N.M. Salem, G.A. Jaleel, A.M. Awwad, Chem. Int., 2020, 6, 137-143.

[2]. T.A.B. Matin, N. Ghasemi, K. Ghodrati, M. Ramezani, Eurasian Chem. Commun., 2019, 1, 494-506.

[3]. S. Taghavi Fardood, F. Moradnia, S. Moradi, R. Forootan, F. Yekke Zare, M. Heidari, Nanochem. Res., 2019, 4, 140-147.

[4]. S. Taghavi Fardood, F. Moradnia, A. Ramazani, Micro & Nano Letters, 2019, 14, 986-991.

[5]. F. Moradnia, S. Taghavi Fardood, A. Ramazani, V. Kumar Gupta, Photobiol, A: Chem., 2020, 392, 112433.

[6]. S. Taghavi Fardood, R. Forootan, F. Moradnia, Z. Afshari, A. Ramazani. Mater. Rese. Express., 2020, 7, 015086

[7]. S. Taghavi Fardood, A. Ramazani, F. Moradnia, Z. Afshari, S. Ganjkhanlu, F. Yekke Zare, Chem. Methodol., 2019, 3, 632-642.

[8]. F. Moradnia, A. Ramazani, S. Taghavi Fardood, F. Gouranlou, Mater. Rese. Express., 2019, 6, 075057.

[9]. A. Ramazani, A. Farshadi, A. Mahyari, F. Sadri, S.W. Joo, P. PAzimzadeh Asiabi, S. Taghavi Fardood, N. Dayyani, H. Ahankar, Int. J. Nano Dimens., 2016, 7, 41-48.

[10]. S. Taghavi Fardood, A. Ramazani, M. Ayubi, M. Moradnia, Sh. Abdpour, R. Forootan, Chemical Methodorrlogies, 2019, 3, 519-525.

[11]. A. Ramazani, A. Mahyari, Helv. Chim. Acta., 2010, 93, 2203-2209.

[12].S. Taghavi Fardood, A. Ramazani, Z. Golfar, S.W. Joo, Applied Organometallic Chemistry, 2017, 31, e3823.

[13]. A.R. Abbasi, H. Kalantary, M. Yousefi, A. Ramazani, A. Morsali, Ultrasonics Sonochemistry, 2012, 19, 853-857.

[14].M. Sorbiun, E. Shayegan Mehr, A. Ramazani, S. Taghavi Fardood, Journal of Materials Science: Materials in Electronics, 2018, 29, 2806-2814.

[15]. K. Atrak, A. Ramazani, S. Taghavi Fardood, Journal of Materials Science: Materials in Electronics, 2018, 29, 6702-6710.

[16]. A. Ramazani, M. Khoobi, F. Sadri, R. Tarasi, A. Shafiee, H. Aghahosseini, S.W. Joo, Appl. Organomet. Chem., 2018, 32, e3908.

[17]. F. Shirini F, M.A. Zolfigol, K. Mohammadi, Bull. Korean Chem. Soc., 2004, 25, 325-327.

[18]. M.B. Mandakea, S.V. Anekarb, S.M. Walke, AIJRSTEM, 2013, 13-25.

[19]. I. Dhimitruka, J. Santa Lucia, Org. Lett., 2006, 8, 47-50.

[20]. N.S. Ahmed Zeki, M.H. Al-Hassani, H.A. Al-Jendeel, Al-Khwarizmi E J., 2010, 6, 33-42.

[21]. M. Xuan, C. Lu, M. Liu, B.L. Lin, J. Org. Chem., 2019, 84, 7694–7701.

[22].B. Neises,W. Steglich, Angew. Chem. Int Ed.,1978, 17, 522–524.

[23]. N.N. Karade, V.H. Budhewar, A.N. Katkar, G.B. Tiwari, ARKIVOC., 2006, xi, 162-167.

[24]. H.Sharghi, M. Hosseini Sarvari, Tetrahedron, 2003, 59, 3627-3633.

[25]. M.A. Zolfigol, E. Madrakian, E. Ghaemi. Molecules, 2002, 7, 734-742.

[26].A.Sakakura, K. Kawajiri, T. Ohkubo, Y. Kosugi Y, K. Ishihara, J Am Chem Soc., 2007, 129, 14775-14779.

[27].C.T.Chen,Y.S. Munot, J. Org. Chem.,2005, 70, 8625-8627.

[28]. M.N. Soltani Rad, S. Behrouz, M.A. Faghihi, A. Khalafi-Nezhad,Tetrahedron Lett., 2008, 49, 1115-1120.

[29]. B.F. Mirjalili, M.A. Zolfigol, A. Bamoniri, Molecules, 2002, 7, 751-755.

[30]. S.D. Le, S. Nishimura, K. Ebitani, Catal. Commun., 2019, 122, 20-23.

[31]. A.R. Modarresi-Alam, M. Nasrollahzadeh, F. Khamooshi, ARKIVOC, 2007, xvi, 238-245.

[32]. S. Pathak, K.D. Ebnath, A. Pramanik, Beilstein J. Org. Chem., 2013, 9, 2344–2353.

[33]. L. Wu1, X. Yang, F. Yan, Bull. Chem. Soc. Ethiop., 2011, 25, 151-155.

How to cite this article: Nahid Ahmadi, Ali Ramazani*, Sobhan Rezayati, Fahimeh Hosseini. Synthesis of silica nanoparticles and study of its catalytic properties in the preparation of carboxylic esters. Eurasian Chemical Communications, 2020, 2(8), 862-874. Link:http://www.echemcom.com/article_108366.html

[34]. D. Shobha, M. Adharvana Chari, K. Mukkanti, K.H. Ahn, J. Heterocyclic. Chem., 2009, 46, 1028-103.

[35]. M. Thommes, K. Katsumi Kaneko, A.V. Neimark, J.P. Olivier, F. Rodriguez-Reinoso, J. Rouquerol, K.S.W. Sing, Pure Appl. Chem. 2015, 87, 1051–106.