scholarly journals Catalytic Performance of SBA-15-Supported Poly (Styrenesulfonic Acid) in the Esterification of Acetic Acid with n-Heptanol

2020 ◽  
Vol 10 (17) ◽  
pp. 5835
Author(s):  
Abdulaziz Ali Alghamdi ◽  
Yahya Musawi Mrair ◽  
Fahad A. Alharthi ◽  
Abdel-Basit Al-Odayni
Keyword(s):  
Acetic Acid ◽  
Sulfonic Acid ◽  
Active Sites ◽  
Structural Characteristics ◽  
High Surface ◽  
High Surface Area ◽  
Reaction Times ◽  
Hydrophobic Surface ◽  
Catalytic Performance ◽  
Catalyst Load

A polystyrene sulfonic acid-functionalized mesoporous silica (SBA-15-PSSA) catalyst was synthesized via an established multistep route, employing 2-bromo-2-methylpropionyl bromide as initiator of atom transfer radical polymerization. Fourier-transform infrared spectroscopy, thermogravimetric/differential thermal, Brunauer–Emmett–Teller, and transmission electron microscopy analyses revealed outstanding structural characteristics of the catalyst, including highly ordered mesopores, high surface area (726 m2/g), and adequate estimated concentrations of active sites (0.70 mmol H+/g). SBA-15-PSSA’s catalytic performance was evaluated in the esterification of acetic acid and n-heptanol as a model system at various temperatures (50–110 °C), catalyst loads (0.1–0.3 g), and reaction times (0–160 min). The conversion percentage of acetic acid was found to increase with the temperature, catalyst load, and reaction time. Furthermore, results indicated a fast conversion in the first 20 min of the reaction, with remarkable conversion values at 110 °C, reaching 86%, 94%, and 97% when the catalyst load was 0.1, 0.2, and 0.3 g, respectively; notably, at this temperature, 100% conversation was achieved after 60 min. At 110 °C, the reaction conducted in the presence of 0.3 g of catalyst displayed more than 6.4 times the efficiency of the uncatalyzed reaction. Such activity is explained by the concomitant presence in the polymer of strong sulfonic acid moieties and a relatively high hydrophobic surface, with adequate numbers of active sites for ester production.

Calcination system-induced nanocasting synthesis of uniform Co3O4 nanoparticles with high surface area and enhanced catalytic performance

RSC Advances ◽  
2015 ◽  
Vol 5 (45) ◽  
pp. 35524-35534 ◽  
Author(s):  
Xiaohong Sun ◽  
Rui You ◽  
Xudong Hu ◽  
Junbin Mo ◽  
Rui Xiong ◽  
...  
Keyword(s):  
Surface Area ◽  
Open System ◽  
Active Sites ◽  
High Surface ◽  
High Surface Area ◽  
Catalytic Performance ◽  
Pore Distribution ◽  
Co3o4 Nanoparticles ◽  
Uniform Size ◽  
Large Pore

Nanoscale Co3O4 synthesized by open-system nanocasting with uniform size, high surface area, large pore-distribution and abundant active-sites exhibited improved catalysis.

Metal-organic-framework derived hollow manganese nickel selenide spheres confined with nanosheets on nickel foam for hybrid supercapacitors

2021 ◽  
Author(s):  
Bahareh ameri ◽  
Akbar Mohammadi Zardkhoshoui ◽  
Saied Saeed Hosseiny Davarani
Keyword(s):  
Active Sites ◽  
Nickel Foam ◽  
Metal Organic Framework ◽  
High Surface ◽  
Metal Organic Frameworks ◽  
High Surface Area ◽  
Supercapacitive Performance ◽  
Hybrid Supercapacitors ◽  
Porous Networks ◽  
Metal Organic

Metal-organic frameworks (MOFs) derived nanoarchitectures have special features, such as high surface area (SA), abundant active sites, exclusive porous networks, and remarkable supercapacitive performance when compared to traditional nanoarchitectures. Herein,...

scholarly journals Sulfamic acid pyromellitic diamide-functionalized MCM-41 as a multifunctional hybrid catalyst for melting-assisted solvent-free synthesis of bioactive 3,4-dihydropyrimidin-2-(1H)-ones

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ehsan Valiey ◽  
Mohammad G. Dekamin ◽  
Zahra Alirezvani
Keyword(s):  
Structural Characteristics ◽  
Biginelli Reaction ◽  
High Surface ◽  
High Surface Area ◽  
Sulfamic Acid ◽  
Solvent Free ◽  
Biologically Active ◽  
Green Protocol ◽  
Solvent Free Conditions ◽  
Mcm 41

AbstractThis study introduces a practical approach to fabricate a novel hybrid acidic catalyst, namely sulfamic acid pyromellitic diamide-functionalized MCM-41 (MCM-41-APS-PMDA-NHSO3H). Various techniques such as FTIR, TGA, XRD, BET, FESEM, and EDX were used to confirm its structural characteristics. The efficiency of the new MCM-41-APS-PMDA-NHSO3H organosilica nanomaterials, as a heterogenous nanocatalyst, was examined in the synthesis of biologically active 3,4-dihydropyrimidin-2-(1H)-one derivatives under solvent-free conditions. It was found that the nanoporous MCM-41-APS-PMDA-NHSO3H, demonstrating acidic nature and high surface area, can activate all the Biginelli reaction components to afford desired 3,4-dihydropyrimidin-2-(1H)-ones under solvent-free conditions in short reaction time. Furthermore, easy and quick isolation of the new introduced hybrid organosilica from the reaction mixture as well as its reusability with negligible loss of activity in at least five consecutive runs are another advantages of this green protocol.

Synthesis and structural characteristics of high surface area TiO2 aerogels by ultrasonic-assisted sol–gel method

2018 ◽  
Vol 29 (7) ◽  
pp. 075702 ◽  
Author(s):  
Feng Qingge ◽  
Cai Huidong ◽  
Lin Haiying ◽  
Qin Siying ◽  
Liu Zheng ◽  
...  
Keyword(s):  
Surface Area ◽  
Structural Characteristics ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Gel Method ◽  
Sol Gel Method ◽  
Ultrasonic Assisted

Efficient and Reusable Silica Gel Supported Metal Ionic Liquid Catalysts for Palmitic Acid Esterification to Biodiesel

2021 ◽  
Vol 43 (1) ◽  
pp. 1-1
Author(s):  
Guo Yingwei Guo Yingwei ◽  
Chen Xuedan Chen Xuedan ◽  
Yan Shiting Yan Shiting ◽  
Zhang Zhengliang Zhang Zhengliang ◽  
Chen Yuqin Chen Yuqin ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Palmitic Acid ◽  
Silica Gel ◽  
High Surface ◽  
High Surface Area ◽  
Kinetic Studies ◽  
Catalytic Performance ◽  
Reaction Conditions ◽  
Acid Esterification ◽  
Supported Metal

A series of silica gel (SG) supported metal ionic liquid catalysts (x[Bmim]Cl-CrCl3/SG) were synthesized and exploited for the esterification of palmitic acid (PA) with methanol (ML) to produce biodiesel efficiently. The 10%[Bmim]Cl-CrCl3/SG catalyst with high surface area and desirable acidity exhibited the best catalytic performance and reusability after six consecutive running cycles. Based on the response surface analysis, the optimal reaction conditions were obtained as follows: methanol/acid mole ratio = 11:1 mol/mol, catalyst amount = 5.3 wt%, reaction time = 65 min, as well as reaction temperature = 373 K, reaching to a biodiesel yield of 96.1%. Further kinetic studies demonstrated that the esterification of PA with ML obeyed 1.41 order kinetics for acid concentration with the activation energy of 16.88 kJ/mol

Engineering Modified Mesoporous Silica Catalysts through Porosity and Surface Acidity Control for Selective Production of DME

2021 ◽  
Vol 894 ◽  
pp. 45-49
Author(s):  
Rosanna Viscardi ◽  
Vincenzo Barbarossa ◽  
Raimondo Maggi ◽  
Francesco Pancrazzi
Keyword(s):  
Mesoporous Silica ◽  
Dimethyl Ether ◽  
Sulfonic Acid ◽  
Pore Diameter ◽  
Solid Acid ◽  
Surface Acidity ◽  
High Surface ◽  
High Surface Area ◽  
Bifunctional Catalysts ◽  
Scanning Electronic Microscopy

DME has been received the attention as a renewable energy due to its thermal efficiencies equivalent to diesel fuel, lower NOx emission, near-zero smoke and non-toxic. DME can be obtained by methanol dehydration over solid acid catalysts or directly from syngas over bifunctional catalysts. The catalytic dehydration of methanol to DME has been widely studied in the literature over pure or modified γ -aluminas (γ-Al2O3) and zeolites. Mesoporous silica has obtained much consideration due to its well-defined structural order, high surface area, and tunable pore diameter. In this work, sulfonic acid and aluminium modified mesoporous silica were synthesized and tested as catalysts for production of dimethyl ether from methanol. The modified silicas were studied utilizing XRD, N2 physisorption, pyridine adsorption, and scanning electronic microscopy. The effects of reaction temperature and water deactivation on the methanol selectivity and conversion to dimethyl ether were investigated. Sulfonic acid modified mesoporous silica showed higher selectivity and stability of DME than that of aluminosilicate. The grafting of mesoporous silica with sulfonic groups displayed much more enhanced hydrothermal stability than Al-MCM-41 and γ-Al2O3.

Spidery catalyst for the synthesis of quinazoline-2,4(1H,3H)-diones

2016 ◽  
Vol 6 (5) ◽  
pp. 1435-1441 ◽  
Author(s):  
Seyed Mohsen Sadeghzadeh
Keyword(s):  
Surface Area ◽  
Active Sites ◽  
High Surface ◽  
High Surface Area

In this study, a novel fibrous nanosilica (KCC-1) based nanocatalyst (Au, Pd, and Cu) with a high surface area and easy accessibility of active sites was successfully developed by a facile approach.

scholarly journals High surface area nitrogen-functionalized Ni nanozymes for efficient peroxidase-like catalytic activity

PLoS ONE ◽  
2021 ◽  
Vol 16 (10) ◽  
pp. e0257777
Author(s):  
Anuja Tripathi ◽  
Kenneth D. Harris ◽  
Anastasia L. Elias
Keyword(s):  
Catalytic Activity ◽  
Plasma Treatment ◽  
Surface Composition ◽  
Point Of Care ◽  
High Surface ◽  
Effective Means ◽  
High Surface Area ◽  
Catalytic Performance ◽  
Optimal Time ◽  
Ammonia Plasma

Nitrogen-functionalization is an effective means of improving the catalytic performances of nanozymes. In the present work, plasma-assisted nitrogen modification of nanocolumnar Ni GLAD films was performed using an ammonia plasma, resulting in an improvement in the peroxidase-like catalytic performance of the porous, nanostructured Ni films. The plasma-treated nanozymes were characterized by TEM, SEM, XRD, and XPS, revealing a nitrogen-rich surface composition. Increased surface wettability was observed after ammonia plasma treatment, and the resulting nitrogen-functionalized Ni GLAD films presented dramatically enhanced peroxidase-like catalytic activity. The optimal time for plasma treatment was determined to be 120 s; when used to catalyze the oxidation of the colorimetric substrate TMB in the presence of H2O2, Ni films subjected to 120 s of plasma treatment yielded a much higher maximum reaction velocity (3.7⊆10−8 M/s vs. 2.3⊆10−8 M/s) and lower Michaelis-Menten coefficient (0.17 mM vs. 0.23 mM) than pristine Ni films with the same morphology. Additionally, we demonstrate the application of the nanozyme in a gravity-driven, continuous catalytic reaction device. Such a controllable plasma treatment strategy may open a new door toward surface-functionalized nanozymes with improved catalytic performance and potential applications in flow-driven point-of-care devices.

Efficient and Reusable Silica Gel Supported Metal Ionic Liquid Catalysts for Palmitic Acid Esterification to Biodiesel

2021 ◽  
Vol 43 (1) ◽  
pp. 1-1
Author(s):  
Guo Yingwei Guo Yingwei ◽  
Chen Xuedan Chen Xuedan ◽  
Yan Shiting Yan Shiting ◽  
Zhang Zhengliang Zhang Zhengliang ◽  
Chen Yuqin Chen Yuqin ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Palmitic Acid ◽  
Silica Gel ◽  
High Surface ◽  
High Surface Area ◽  
Kinetic Studies ◽  
Catalytic Performance ◽  
Reaction Conditions ◽  
Acid Esterification ◽  
Supported Metal

A series of silica gel (SG) supported metal ionic liquid catalysts (x[Bmim]Cl-CrCl3/SG) were synthesized and exploited for the esterification of palmitic acid (PA) with methanol (ML) to produce biodiesel efficiently. The 10%[Bmim]Cl-CrCl3/SG catalyst with high surface area and desirable acidity exhibited the best catalytic performance and reusability after six consecutive running cycles. Based on the response surface analysis, the optimal reaction conditions were obtained as follows: methanol/acid mole ratio = 11:1 mol/mol, catalyst amount = 5.3 wt%, reaction time = 65 min, as well as reaction temperature = 373 K, reaching to a biodiesel yield of 96.1%. Further kinetic studies demonstrated that the esterification of PA with ML obeyed 1.41 order kinetics for acid concentration with the activation energy of 16.88 kJ/mol

scholarly journals Catalytic Cracking of n-Hexadecane Using Carbon Nanostructures/Nano-Zeolite-Y Composite Catalyst

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1385
Author(s):  
Botagoz Zhuman ◽  
Shaheen Fatima Anis ◽  
Saepurahman ◽  
Gnanapragasam Singravel ◽  
Raed Hashaikeh
Keyword(s):  
Surface Area ◽  
Catalytic Cracking ◽  
Carbon Nanostructures ◽  
Active Sites ◽  
Zeolite Y ◽  
High Surface ◽  
High Surface Area ◽  
Composite Catalyst ◽  
Homogeneous Distribution ◽  
Binding Material

Zeolite-based catalysts are usually utilized in the form of a composite with binders, such as alumina, silica, clay, and others. However, these binders are usually known to block the accessibility of the active sites in zeolites, leading to a decreased effective surface area and agglomeration of zeolite particles. The aim of this work is to utilize carbon nanostructures (CNS) as a binding material for nano-zeolite-Y particles. The unique properties of CNS, such as its high surface area, thermal stability, and flexibility of its fibrous structure, makes it a promising material to hold and bind the nano-zeolite particles, yet with a contemporaneous accessibility of the reactants to the porous zeolite structure. In the current study, a nano-zeolite-Y/CNS composite catalyst was fabricated through a ball milling approach. The catalyst possesses a high surface area of 834 m2/g, which is significantly higher than the conventional commercial cracking catalysts. Using CNS as a binding material provided homogeneous distribution of the zeolite nanoparticles with high accessibility to the active sites and good mechanical stability. In addition, CNS was found to be an effective binding material for nano-zeolite particles, solving their major drawback of agglomeration. The nano-zeolite-Y/CNS composite showed 80% conversion for hexadecane catalytic cracking into valuable olefins and hydrogen gas, which was 14% higher compared to that of pure nano-zeolite-Y particles.

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