scholarly journals MODIFICATION OF EXPANDED PERLITE WITH ORTHOPHENANTHROLINE FOR FORMATION OF ACTIVE SITES FOR ACID DYES: PREPARATION AND CHARACTERIZATION

2018 ◽  
Vol 15 (30) ◽  
pp. 338-346
Author(s):  
J. M. F. ALMEIDA ◽  
I. N. SILVA ◽  
E. DAMASCENO JUNIOR ◽  
N. S. FERNANDES
Keyword(s):  
Mass Loss ◽  
Active Sites ◽  
Amorphous Material ◽  
Xrd Analysis ◽  
Acid Sites ◽  
Lewis Base ◽  
Expanded Perlite ◽  
Acid Dyes ◽  
Oh Groups ◽  
Thermogravimetric Curve

The expanded perlite (aluminosilicate naturally acid) has been modified with orthophenanthroline (Lewis base). The material was characterized by TG/DTA, XRD and IR. The thermogravimetric curve of the modified expanded perlite presented a lower thermal stability due to the orthophenanthroline and showed 13,6% of mass loss total. However, pure expanded perlite presented only 2,3% of the mass loss. The DTA curve showed endothermic event characteristic of the presence of orthophenanthroline. For XRD analysis is visualized, the presence of reflections in the diffractogram relating to the modified material of orthophenanthroline peaks of crystallinity since no modification perlite is an amorphous material. The band regarding absorption vibration of Si-O group appears at lower wavenumbers than in the unmodified material. So there was an interaction between the OH groups of silanols of perlite groups with unshared electron pairs of nitrogen atoms and C=C bonds (also rich in electrons) in the chemical structure of orthophenanthroline as a result of a hydrogen bond between these groups. thus perlite was modified through the interaction of its acid sites (Si-OH) with Lewis basic sites of orthophenanthroline.

The Effect of Acidity of Al and Fe Silicates with MFI Structure on Benzene and Toluene Alkylation with Isopropyl Alcohol

1996 ◽  
Vol 61 (8) ◽  
pp. 1115-1130 ◽  
Author(s):  
Jiří Čejka ◽  
Naděžda Žilková ◽  
Blanka Wichterlová
Keyword(s):  
Kinetic Study ◽  
Molecular Sieves ◽  
Isopropyl Alcohol ◽  
Acid Sites ◽  
Transport Rate ◽  
Reaction Products ◽  
Oh Groups ◽  
Benzene Alkylation ◽  
Toluene Alkylation ◽  
Low Strength

Kinetic study of toluene and benzene alkylation with isopropyl alcohol on alumo- and ferrisilicates of MFI structure has shown that the alkylation activity does not follow the acidity (both the number and strength of bridging OH groups) of these molecular sieves. The rate of the overall reaction is controlled by the desorption/transport rate of bulky, strongly adsorbed cymenes and cumene. A higher concentration of n-propyltoluenes compared to n-propylbenzene, both undesired reaction products, formed via a bimolecular isomerization of isopropyl aromate with benzene or toluene, was due to the higher reactivity of isopropyltoluene with toluene in comparison with that of cumene with benzene. It is concluded that ferrisilicates of MFI structure possessing low strength acid sites appear to be promising catalysts for achieving both a high isopropyl- and para-selectivity in toluene alkylation to p-cymene.

A study on using expanded perlite with hydroxyapatite: Reinforced bio-composites

2021 ◽  
pp. 095441192199656
Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu
Keyword(s):  
Body Fluid ◽  
Xrd Analysis ◽  
Cold Isostatic Pressing ◽  
Expanded Perlite ◽  
X Ray Diffraction ◽  
Pressing Method ◽  
X Ray ◽  
Infra Red ◽  
Ft Ir

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.

scholarly journals On the Role of Protonic Acid Sites in Cu Loaded FAU31 Zeolite as a Catalyst for the Catalytic Transformation of Furfural to Furan

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 2015
Author(s):  
Łukasz Kuterasiński ◽  
Małgorzata Smoliło-Utrata ◽  
Joanna Kaim ◽  
Wojciech Rojek ◽  
Jerzy Podobiński ◽  
...  
Keyword(s):  
Active Sites ◽  
Acid Sites ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Brønsted Acid Sites ◽  
Protonic Acid ◽  
Brönsted Acid ◽  
Brönsted Acid Sites ◽  
Bronsted Acid Sites

The aim of the present paper is to study the speciation and the role of different active site types (copper species and Brønsted acid sites) in the direct synthesis of furan from furfural catalyzed by copper-exchanged FAU31 zeolite. Four series of samples were prepared by using different conditions of post-synthesis treatment, which exhibit none, one or two types of active sites. The catalysts were characterized by XRD, low-temperature sorption of nitrogen, SEM, H2-TPR, NMR and by means of IR spectroscopy with ammonia and CO sorption as probe molecules to assess the types of active sites. All catalyst underwent catalytic tests. The performed experiments allowed to propose the relation between the kind of active centers (Cu or Brønsted acid sites) and the type of detected products (2-metylfuran and furan) obtained in the studied reaction. It was found that the production of 2-methylfuran (in trace amounts) is determined by the presence of the redox-type centers, while the protonic acid sites are mainly responsible for the furan production and catalytic activity in the whole temperature range. All studied catalysts revealed very high susceptibility to coking due to polymerization of furfural.

scholarly journals Control of zeolite microenvironment for propene synthesis from methanol

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Longfei Lin ◽  
Mengtian Fan ◽  
Alena M. Sheveleva ◽  
Xue Han ◽  
Zhimou Tang ◽  
...  
Keyword(s):  
Active Sites ◽  
Inelastic Neutron Scattering ◽  
Sustainable Manufacturing ◽  
Methanol Conversion ◽  
Acid Sites ◽  
Light Olefins ◽  
Carbon Bond ◽  
X Ray ◽  
Carbon Carbon Bond ◽  
Catalytic Stability

AbstractOptimising the balance between propene selectivity, propene/ethene ratio and catalytic stability and unravelling the explicit mechanism on formation of the first carbon–carbon bond are challenging goals of great importance in state-of-the-art methanol-to-olefin (MTO) research. We report a strategy to finely control the nature of active sites within the pores of commercial MFI-zeolites by incorporating tantalum(V) and aluminium(III) centres into the framework. The resultant TaAlS-1 zeolite exhibits simultaneously remarkable propene selectivity (51%), propene/ethene ratio (8.3) and catalytic stability (>50 h) at full methanol conversion. In situ synchrotron X-ray powder diffraction, X-ray absorption spectroscopy and inelastic neutron scattering coupled with DFT calculations reveal that the first carbon–carbon bond is formed between an activated methanol molecule and a trimethyloxonium intermediate. The unprecedented cooperativity between tantalum(V) and Brønsted acid sites creates an optimal microenvironment for efficient conversion of methanol and thus greatly promotes the application of zeolites in the sustainable manufacturing of light olefins.

Adsorption of Benzene from Aqueous Solution Using Base Modified Expanded Perlite

2012 ◽  
Vol 622-623 ◽  
pp. 1779-1783
Author(s):  
Richard Appiah-Ntiamoah ◽  
Xuan Thang Mai ◽  
Francis W.Y. Momade ◽  
Hern Kim
Keyword(s):  
Zeta Potential ◽  
Adsorption Capacity ◽  
Linear Regression Analysis ◽  
Basic Medium ◽  
Maximum Adsorption Capacity ◽  
Hydroxyl Groups ◽  
Expanded Perlite ◽  
Oh Groups ◽  
Base Solution ◽  
Ph Range

In this study, the adsorption capacity of expanded perlite (EP) for benzene at low concentrations in water was investigated after EP was treated with sodium hydroxide (NaOH). IR spectra used to characterize the modified EP showed that there was no bonding between NaOH and the hydroxyl groups on the surface of EP. However, the NaOH provided a basic medium for negatively charged surface oxide ions (-SO-) to form on EP. This fact was corroborated by pH readings of the modification solution. This reduced in pH from 10 to 9 at the end of the reaction which indicated that the hydroxyl OH- groups on the EP underwent deprotonation and hence releases H+ into the solution, and also positive sites on EP adsorbed OH- ions from the base solution. Mahir et al. in their paper Zeta potential of unexpanded and expanded perlite samples in various electrolyte media confirmed that EP has no isoelectric point and exhibits negative zeta potential in the pH range of 2-11. The surface oxides (-SO-) were believed to have given EP it adsorptive potential. Adsorption isotherm values correlated reasonably well with the Langmuir isotherm model and it parameters (qo and K) were obtained using linear regression analysis. A maximum adsorption capacity (qo) value of 19.42 mg/g was achieved.

THE USE OF THE COMBINATION OF FTIR, PYRIDINE ADSORPTION, 27Al AND 29Si MAS NMR TO DETERMINE THE BRÖNSTED AND LEWIS ACIDIC SITES

2016 ◽  
Vol 78 (6) ◽  
Author(s):  
Djoko Hartanto ◽  
Lai Sin Yuan ◽  
Sestriana Mutia Sari ◽  
Djarot Sugiarso ◽  
Irmina Kris Murwarni ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Aluminum Atom ◽  
Xrd Analysis ◽  
Acid Sites ◽  
Mas Nmr ◽  
Molar Ratio ◽  
Pyridine Adsorption ◽  
Lewis Acid Sites ◽  
27Al Mas Nmr ◽  
Pre Treatment

Lewis and Brönsted acidity were studied on ZSM-5 with combination of pyridine adsorption and FTIR vibration, ZSM-5 synthesized using kaolin Bangka Indonesia with an increase in the molar ratio of Si/Al 30-60 without pre-treatment and without organic templates and with seeds silicalite. Interestingly, the intensity of the infrared showed an increase of band vibration pyridine as absorbed Brönsted and Lewis acid sites in a molar ratio increase of Si/Al in ZSM-5, indicating an increase in the number of silanol (Brönsted acid) and deformed silica (Lewis acid) because the amount of Aluminum in ZSM-5 decrease with increase Si/Al but amount acidity increase. 29Si and 27Al MAS NMR analysis was supported by the results of infrared to indicate that all of the aluminum atom is coordinated with their neighbors are the same in ordering the ZSM-5 framework and 27Al MAS NMR showed a sharp peak of all the variations of Si/Al except the Si/Al 30 shows a low peak area. XRD analysis supported that the ZSM-5 structure formed is pure and crystal and a decrease in crystallinity proven for more than Si/Al 50, that defects silica occurs in ZSM-5, this corresponds to the growing number of Lewis acid sites caused by defects silica described the infrared results.

The structure and activity of potassium supported on SBA-15 molecular sieve: Density functional theory study

2014 ◽  
Vol 13 (01) ◽  
pp. 1350076 ◽  
Author(s):  
Bing Liu ◽  
Daxi Wang ◽  
Zhongxue Wang ◽  
Zhen Zhao ◽  
Yu Chen ◽  
...  
Keyword(s):  
Density Functional Theory ◽  
Lewis Acid ◽  
Molecular Sieve ◽  
Active Sites ◽  
Density Functional ◽  
Structural Model ◽  
Vibrational Frequencies ◽  
Oxygen Molecule ◽  
Lewis Base ◽  
Functional Theory

The geometries, vibrational frequencies, electronic properties and reactivity of potassium supported on SBA-15 have been theoretically investigated by the density functional theory (DFT) method. The structural model of the potassium supported on SBA-15 was constructed based on our previous work [Wang ZX, Wang DX, Zhao Z, Chen Y, Lan J, A DFT study of the structural units in SBA-15 mesoporous molecular sieve, Comput. Theor. Chem.963, 403, 2011]. This paper is the extension of our previous work. The most favored location of potassium atom was obtained by the calculation of substitution energy. The calculated vibrational frequencies of K /SBA-15 are in good agreement with the experimental results. By analyzing the properties of electronic structure, we found that the O atom of Si - O (2)- K group acts as the Lewis base center and the K atom acts as the Lewis acid center. The reactivity of K /SBA-15 was investigated by calculating the activation of oxygen molecule. The oxygen molecule can be activated by K /SBA-15 with an energy barrier of 103.2 kJ/mol. In the final state, the activated oxygen atoms become new Lewis acid centers, which are predicted to act as the active sites in the catalytic reactions. This study provides a deep insight into the properties of supported potassium catalysts and offers fundamental information for further research.

scholarly journals Adsorption of aquatic Cd2+ using a combination of bacteria and modified carbon fiber

2017 ◽  
Vol 36 (3-4) ◽  
pp. 857-871 ◽  
Author(s):  
Chao Xue ◽  
Peishi Qi ◽  
Yunzhi Liu
Keyword(s):  
Aqueous Solution ◽  
Composite Material ◽  
Carbon Fiber ◽  
Active Sites ◽  
Ph Value ◽  
Removal Rate ◽  
Sorption Process ◽  
Acid Sites ◽  
Heterogeneous Distribution ◽  
Carbon Fiber Material

Batch experiments were conducted to investigate the capacity and mechanisms for adsorbing Cd2+ from aqueous solutions by the composite material. The composite material was manufactured with Plesiomonas shigelloides strain H5 and modified polyacrylonitrile-based carbon fiber. Experimental results showed that the surface areas of modified polyacrylonitrile-based carbon fiber increased by 58.54% and pore width increased by 40.19% compared with unmodified polyacrylonitrile-based carbon fiber. Boehm’s titration results show the surface acid sites of composite material were increased by 712% compared with unmodified polyacrylonitrile-based carbon fiber. The field emission scanning electron microscope results show P. shigelloides H5 can be grown on the surface of modified polyacrylonitrile-based carbon fiber closely. The equilibrium removal rate and sorption quantity of composite material were 71.56% and 7.126 mg g−1, respectively. With the pH value of aqueous solution increased, the removal rate of Cd2+ ions was also increased, but the change of temperature and ionic strength had no significant effect on the removal rate. Furthermore, the results showed the whole sorption process was a good fit to Lagergren pseudo-second-order model and Freundlich isotherms model. Therefore, the results infer that there was a heterogeneous distribution of active sites, and then the sorption process was chemical adsorption and multilayer adsorption. In a word, microbial composite carbon fiber material can adsorb Cd2+ ions from aqueous solution effectively, which might be helpful in wastewater treatment in the future.

scholarly journals The Role of Polypropylene Microfibers in Thermal Properties and Post-Heating Behavior of Cementitious Composites

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2676
Author(s):  
Mohammad R. Irshidat ◽  
Nasser Al-Nuaimi ◽  
Mohamed Rabie
Keyword(s):  
Melting Point ◽  
Heat Flow ◽  
Mass Loss ◽  
Failure Modes ◽  
Cement Mortar ◽  
Xrd Analysis ◽  
Cementitious Composites ◽  
Polypropylene Fibers ◽  
Scanning Calorimetry ◽  
Heating Behavior

This paper experimentally studied the effect of polypropylene (PP) microfibers on thermal and post-heating mechanical behaviors of cementitious composites. Cement mortars with small dosage of polypropylene fibers were prepared, heated at various temperatures (150 °C, 200 °C, 450 °C, and 600 °C), and then tested. The investigated parameters include residual compressive and flexural strengths, elastic modulus, fracture energy, stress intensity factors, failure modes, microstructure (scanning electron microscopy (SEM) imaging), thermal conductivity, heat flow (differential scanning calorimetry (DSC) test), mass loss (thermogravimetric analysis (TGA) test), and chemical composition (XRD analysis). The results showed the efficiency of PP fibers to enhance the post-heating behavior and the residual mechanical properties of cement mortar after heating. The presence of PP fibers did not affect the heat flow and the mass loss of cement mortar at room temperature. However, heating cement mortar at temperature beyond the melting point of the fibers negatively affected its thermal behavior. The presence of PP fibers played a major role in bridging the cracks and mitigating their propagation. Once the melting point of the polypropylene fibers is exceeded, the fibers melted and created extra voids in the microstructure of concrete.

scholarly journals The ZSM-5-Catalyzed Oxidation of Benzene to Phenol with N2O: Effect of Lewis Acid Sites

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 44
Author(s):  
Cui Ouyang ◽  
Yingxia Li ◽  
Jianwei Li
Keyword(s):  
Active Sites ◽  
Acid Sites ◽  
X Ray Diffraction ◽  
Remarkable Feature ◽  
Chemisorbed Oxygen ◽  
Lewis Acidic Sites ◽  
Acidic Sites ◽  
Adsorption Desorption ◽  
Oxidation Of Benzene ◽  
N2o Selectivity

The oxidation of benzene to phenol (BTOP) with N2O as the oxidant has been studied with a variety of Fe/ZSM-5 catalysts. The literature has conclusively proven that Fe2+ sites are the active sites. However, some studies have suggested that the Lewis acidic sites (LAS) are responsible for the generation of the active chemisorbed oxygen. Nevertheless, there is no clear relationship between the LAS and the N2O selectivity to phenol. In an effort to elucidate the effects of LAS on BTOP with various ZSM-5 catalysts, we investigated the initial N2O selectivity to phenol. Here we show that the initial N2O selectivity to phenol is negative with the amount of LAS over a certain range. The catalyst H-ZSM-5-ST (H-ZSM-5 treated with water vapor) showed a remarkable initial N2O selectivity to phenol as high as 95.9% with a 0.021 mmol g−1 LAS concentration on the surface of the catalyst, while the Fe/ZSM-5 catalyst demonstrated the lowest initial N2O selectivity to phenol (11.7%) with the highest LAS concentration (0.137 mmol g−1). Another remarkable feature is that steaming was more effective than Fe ion exchange and high temperature calcining. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), N2-adsorption-desorption, UV-vis, NH3-TPD and pyridine Fourier transform infrared (FT-IR) techniques. Our results demonstrate how the concentration of LAS is likely to affect the initial N2O selectivity to phenol within a certain range (0.021–0.137 mmol g−1). This research has demonstrated the synergy between the active Fe2+ sites and LAS.

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