scholarly journals Preparation of mesoporous zirconium incorporated MCM-48 solid acid catalyst and its catalytic activity for alkylation of phenol with tert-butyl alcohol

Author(s):  
Tingshun Jiang ◽  
Yan Ma ◽  
Jinlian Cheng ◽  
Wangping Liu ◽  
Xuping Zhou ◽  
...  
2018 ◽  
Vol 3 (2) ◽  
pp. 801-808 ◽  
Author(s):  
Lakshmy Muraleedharan ◽  
Bellundagere ◽  
M. Chandrashekara ◽  
Bangalore ◽  
S. Jai Prakash ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (25) ◽  
pp. 19652-19658 ◽  
Author(s):  
An-Qi Wang ◽  
Xiu-Ling Wu ◽  
Jun-Xia Wang ◽  
Hui Pan ◽  
Xiao-Yun Tian ◽  
...  

A new spinel-style S2O82−/ZnAl2O4 catalyst with the mesoporous structure exhibited the well catalytic activity and structural stability.


Author(s):  
Ganapati D. Yadav ◽  
Shashikant B Kamble

Alkylation of mesitylene with tert-butyl alcohol in the presence of novel mesoporous superacidic catalysts, namely, UDCaT-4, UDCaT-5 and UDCaT-6 was investigated. The catalysts are modified versions of zirconia showing high catalytic activity, stability and reusability in the presence of water as compared to conventional sulfated zirconia. The catalytic activity is in the order: UDCaT-5 (most active) > UDCaT-6 > UDCaT-4 > sulfated zirconia (S-ZrO2) (least active). The synergistic effect of the very high sulfur content present (9% w/w S) and the preservation of the tetragonal phase in UDCaT-5, in comparison with sulfated zirconia (4% w/w S), were responsible for higher catalytic activity. A catalyst ensuring the production of 2-tert-butyl-mesitylene (2-TBMT) with 98% selectivity and 94% conversion of tert-butanol (TBA) was developed under optimum reaction conditions. The formation of products is correlated with the acidity of the catalyst. The reactions were conducted in liquid phase at relatively low reaction temperatures (120–150 °C). A systematic investigation of the effects of various operating parameters was accomplished and a mathematical model is developed to describe the reaction pathway and validated with experimental results. The reaction was carried out without using any solvent in order to make the process cleaner and greener. An overall second order kinetic equation was used to fit the experimental data, under the assumption that both mesitylene and tert-butanol are weakly adsorbed. An independent dehydration study of tert-butanol (TBA) was also done.


2019 ◽  
Vol 7 (1) ◽  
pp. 55-80 ◽  
Author(s):  
Fatemeh Ghorbani ◽  
Seied Ali Pourmousavi ◽  
Hamzeh Kiyani

Background: Much attention has been focused on heterogeneous catalysts. Reactions with these recoverable and reusable catalysts are clean, selective with high efficiency. Among the heterogeneous solid acid catalyst in organic synthesis, Carbon-Based Solid Acids (CBSAs), which are important solid acid with many practical and research applications have been extensively studied. In this work, green Pistachio peel, a biomass waste, was converted into a novel carbon-based solid acid catalyst (Pis-SO3H). Objective: The aim of this work is to synthesize highly sulfonated carbon as an efficient, recyclable, nontoxic solid acid catalyst by simultaneous sulfonation, dehydration and carbonization of green Pistachio peel as biomass and investigate the catalytic activity of Pis-SO3H in acetalization, thioacetalization, acylation of aldehydes and synthesis of 3,3'-Arylmethylene-bis(4-hydroxycoumarin) derivatives. Method: Pis-SO3H was synthesized by an integrated fast one-step hydrothermal carbonization and sulfonation process in the presence of sulfuric acid. The characterization of the physicochemical properties of Pis-SO3H was achieved by XRD, FT-IR, FE-SEM, and elemental analysis. Results: The result of acid-base titration showed that the total acidity of the catalyst was 7.75 mmol H+g−1. This new heterogeneous catalyst has been efficiently used for the chemoselective thioacetalization, acetalization and acylation of aldehyde and the synthesis of biscoumarins under solvent-free conditions. All the reactions work easily in high yields. The antimicrobial activity of some of the biscoumarins was evaluated in screening by disk diffusion assay for the zone of inhibition. Conclusion: The catalytic activity of the Pis-SO3H was investigated during acetalization, thioacetalization, acylation and synthesis of biscoumarins. The results of protection of carbonyl groups and synthesis of biscoumarins in the present work offer effective alternatives for environmentally friendly utilization of abundant biomass waste.


2011 ◽  
Vol 383-390 ◽  
pp. 1144-1149 ◽  
Author(s):  
Yue Ling Gu ◽  
Guo Hui Xu ◽  
Zuo Gang Guo ◽  
Shu Rong Wang

Solid acid catalyst has high catalytic esterification activity but with a free acid excess problem. In this paper, washing pretreatments were adopted in the catalyst preparation processes and their influences on catalytic activity and residual free acid amount were investigated. Residual free acid amount can be reduced by 33% with both washing before calcinations and washing after calcinations pretreatments. But their influences on catalyst activities were different. Washing before calcinations pretreatment reduced the catalytic activity from 80.29% to 57.72% while the other washing pretreatment had little influence on the catalyst activity. In order to describe the influence mechanism of washing pretreatments, catalysts were characterized by FT-IR and XRD. Finally, typical compounds in bio-oil were selected to form a bio-oil model compounds system. The catalyst pretreated by washing after calcinations was used on the esterification research of this bio-oil model system. The volume ratio of propanol to bio-oil model compound was 3:1. The reaction temperature was 90 °C and the amount of catalyst was 2wt% of total liquid mass. Combined with the GC-MS qualitative and quantitative results, carboxylic acids, such as formic acid, acetic acid, propionic acid were converted to esters effectively.


2015 ◽  
Vol 41 (9) ◽  
pp. 12186-12191 ◽  
Author(s):  
Qiang Zhao ◽  
Shuangming Meng ◽  
Junli Wang ◽  
Yongsheng Qiao ◽  
Zuopeng Li ◽  
...  

2010 ◽  
Vol 96 ◽  
pp. 183-187 ◽  
Author(s):  
Pan Wang ◽  
Si Hui Zhan ◽  
Hong Bing Yu

Using solid acid catalyst for the levulinic acid (LA) production from cellulose is one of the promising methods for utilization of biomass. An environmentally friendly solid acid catalyst, sulfated TiO2 was prepared by precipitation-impregnation method and used to catalyze the production of levulinic acid from cellulose. The concentration of sulphuric acid had a remarkable influence on the construction and catalytic activity of sulfated TiO2. The influence of reaction temperature and catalyst dosage on levulinic acid yield was also investigated with the aim to obtain the highest yield of LA. The optimum condition for the highest yield of levulinic acid (27.2%) was achieved at 240 °C, 0.7g of sulfated TiO2 and reaction time of 15 min. The recycling test indicated that the catalytic activity of the catalyst had a slight decrease after being used two times.


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