scholarly journals Activation and Characterization of Algerian Kaolinite, New and Green Catalyst for Synthesis of Polystyrene and Poly(1,3-dioxolane)

2021 ◽  
Vol 15 (4) ◽  
pp. 551-558
Author(s):  
Sarra Sabrina Aiche ◽  
◽  
Hodhaifa Derdar ◽  
Zakaria Cherifi ◽  
Mohammed Belbachir ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Reaction Time ◽  
1H Nmr ◽  
Room Temperature ◽  
Exchange Process ◽  
Sem Analysis ◽  
Green Catalyst ◽  
Modified Clay ◽  
Calculated Molecular Weight ◽  
Ft Ir

In the present work we have explored a new catalyst prepared with Algerian clay and a new method to synthesise polystyrene and poly(1,3-dioxolane). This technique consists of using Algerian modified clay (Kaolinite-H+) as a green catalyst. Kaolinite-H+ is a proton exchanged clay which is prepared through a simple exchange process. Synthesis experiments are performed in bulk. The polymerization of styrene in bulk leads to the yield of 83 % at room temperature with the reaction time of 3 h. Molecular weight of the obtained polystyrene is calculated by 1H NMR and is about 2196 g/mol. Polymerization of (1,3-dioxolane) is carried out at room temperature with the reaction time of 3 h and polymerization yield of 91 %. The calculated molecular weight of the obtained poly(1,3-dioxolane) is about 573 g/mol. The structure of the obtained polymers is confirmed by FT-IR and 1H NMR. The modified clay (Kaolinite-H+) is characterized by FT-IR, XRD and SEM analysis.

scholarly journals Polymerization of Ethylene Glycol Dimethacrylate (EGDM), Using An Algerian Clay as Eco-catalyst (Maghnite-H+ and Maghnite-Na+)

2020 ◽  
Vol 15 (1) ◽  
pp. 221-230 ◽  
Author(s):  
Sara Haoue ◽  
Hodhaifa Derdar ◽  
Mohammed Belbachir ◽  
Amine Harrane
Keyword(s):  
Ethylene Glycol ◽  
Exchange Process ◽  
Ethylene Glycol Dimethacrylate ◽  
Glycol Dimethacrylate ◽  
Green Catalyst ◽  
Ion Exchange Process ◽  
Ft Ir ◽  
Uv Visible ◽  
Thermal Stability Of ◽  
End Group

In this paper we have explored a novel and green method to synthesis and polymerize ethylene glycol dimethacrylate (EGDM). This technique consists on using Maghnite (Algerian clay) as a green catalyst to replace toxic catalysts. The Algerian clay has been modified using two ion exchange process to obtain Maghnite-H+ (proton exchanged process) and Maghnite-Na+ (sodium exchanged process). Synthesis experiments of EGDM and Poly (EGDM) are performed in bulk respecting the principles of green chemistry. The structure of the obtained monomer and the obtained polymer was confirmed by FT-IR, 1H-NMR and 13C-NMR, where the methacrylate end groups are clearly visible. The presence of unsaturated end group in the structure of monomer was confirmed by UV-Visible analysis. Thermogravimetric analysis (TGA) was used to study the thermal stability of these obtained products. Copyright © 2020 BCREC Group. All rights reserved 

scholarly journals Synthesis of Propylene Oxide – Styrene Copolymers

2021 ◽  
Vol 10 (3) ◽  
pp. 2389-2395
Keyword(s):  
Propylene Oxide ◽  
Room Temperature ◽  
Structural Characteristics ◽  
Exchange Process ◽  
Proton Exchange ◽  
Styrene Copolymers ◽  
Forward Proton ◽  
Ft Ir ◽  
Ubbelohde Viscometer ◽  
Ft Ir Spectroscopy

The copolymerization of propylene oxide (PO) with styrene (St) catalyzed by Maghnite-H+ (Mag-H+) was investigated. Mag-H+, a nontoxic catalyst for cationic polymerization of vinylic and heterocyclic monomers, is a montmorillonite silicate sheet clay. This catalyst was prepared through a straight forward proton exchange process. It was found that Mag-H+ initiates the copolymerization in bulk at room temperature. Various techniques, including H1NMR, 13C-NMR, FT-IR spectroscopy, and Ubbelohde viscometer, were used to elucidate the resulting copolymers' structural characteristics. The effects of the amount of Mag-H+ and propylene oxide were studied. The yield of copolymerization depends on the amount of Mag-H+ used and the reaction time.

scholarly journals A Green Synthesis of Polylimonene Using Maghnite-H+, an Exchanged Montmorillonite Clay, as Eco-Catalyst

2019 ◽  
Vol 14 (1) ◽  
pp. 69 ◽  
Author(s):  
Hodhaifa Derdar ◽  
Mohammed Belbachir ◽  
Amine Harrane
Keyword(s):  
Reaction Time ◽  
Green Synthesis ◽  
Exchange Process ◽  
Gel Permeation Chromatography ◽  
Bulk Polymerization ◽  
Montmorillonite Clay ◽  
Scanning Calorimetry ◽  
Reaction Conditions ◽  
Ft Ir ◽  
Optimal Reaction

A new green polymerization technique to synthesis polylimonene (PLM) is carried out in this work. This technique consists of using Maghnite-H+ as eco-catalyst to replace Friedel-Crafts catalysts which are toxics. Maghnite-H+ is a montmorillonite silicate sheet clay which is prepared through a simple exchange process. Polymerization experiments are performed in bulk and in solution using CH2Cl2 as solvent. Effect of reaction time, temperature and amount of catalyst is studied, in order to find the optimal reaction conditions. The polymerization in solution leads to the best yield (48.5%) at -5°C for a reaction time of 6 h but the bulk polymerization, that is performed at 25°C, remains preferred even if the yield is lower (40.3%) in order to respect the principles of a green chemistry which recommend syntheses under mild conditions, without solvents and at room temperature. The structure of the obtained polymer (PLM) is confirmed by FT-IR and Nuclear Magnetic Resonance of proton (1H-NMR). The glass transition temperature (Tg) of the polylimonene is defined using Differential Scanning Calorimetry (DSC) and is between 113°C and 116°C. The molecular weight of the obtained polymer is determined by Gel Permeation Chromatography (GPC) analysis and is about 1360 g/mol. Copyright © 2019 BCREC Group. All rights reservedReceived: 26th May 2018; Revised: 11st September 2018; Accepted: 22nd September 2018; Available online: 25th January 2019; Published regularly: April 2019How to Cite: Derdar, H., Belbachir, M., Harrane, A. (2019). A Green Synthesis of Polylimonene Using Maghnite-H+, an Exchanged Montmorillonite Clay, as Eco-Catalyst. Bulletin of Chemical Reaction Engineering & Catalysis, 14 (1): 69-78 (doi:10.9767/bcrec.14.1.2692.69-78)Permalink/DOI: https://doi.org/10.9767/bcrec.14.1.2692.69-78 

Synthesis of Microcrystalline Cellulose Grafting Poly (methyl methacrylate) Copolymers by ATRP in 1-Allyl-3-Methylimidazolium Chloride

2012 ◽  
Vol 621 ◽  
pp. 157-161 ◽  
Author(s):  
Er Jun Tang ◽  
Miao Yuan ◽  
Liang Li ◽  
Feng Bian ◽  
Di Shun Zhao
Keyword(s):  
Molecular Weight ◽  
Ionic Liquid ◽  
Methyl Methacrylate ◽  
Atom Transfer Radical Polymerization ◽  
Radical Polymerization ◽  
1H Nmr ◽  
Microcrystalline Cellulose ◽  
Methacrylate Copolymers ◽  
Covalently Bonded ◽  
Ft Ir

The microcrystalline cellulose grafting polymethylmethacrylate (MCC-g-PMMA) copolymer was successfully synthesized by atom transfer radical polymerization (ATRP) using ethanediamine as ligand in Ionic liquid 1-allyl-3-methylimidazolium chloride ([AMIM]Cl). The MCC-g-PMMA was characterized by FT-IR, 1H NMR, SEM and GPC spectroscopies. The results confirmed that the PMMA had been covalently bonded to cellulose backbone. The molecular weight of graft copolymers linearly increased during the polymerization and presented a low polydispersity.

Preparation of Nano-MnO2 and Adsorption of Reactive Brilliant Blue

2016 ◽  
Vol 847 ◽  
pp. 294-298
Author(s):  
Xiao Feng Fan ◽  
Yue Cheng
Keyword(s):  
Reaction Time ◽  
Room Temperature ◽  
Particle Diameter ◽  
Solution Concentration ◽  
Brilliant Blue ◽  
Uniform Size ◽  
Initial Concentration ◽  
One Step ◽  
Ft Ir ◽  
Xrd Patterns

MnO2 nanoparticles were prepared by one-step redox under room temperature. The sample was characterized by XRD, SEM, TEM and FT-IR. The results indicated that the MnO2 nanoparticles was amorphous δ-MnO2 with the uniform size of 10-20nm in particle diameter, which can be seen by XRD patterns. The four peaks appear at 2θ = 23.24°,36.1°,45.42°and 64.38°, respectively. FT-IR results showed the 519 cm-1 as Mn-O features manganese dioxide absorption. The effect of the pH, nanoMnO2 dosage, reaction time, reaction temperature and initial concentration were studied on the removal of reactive brilliant blue. It was found that the removal ability of reactive brilliant blue was the best under the selected conditions: pH was 3.0, dosage of nanoMnO2 was 0.05g, KN-R solution concentration was 5mg / L, reaction time was 2h, temperature was 25°C.

The Removal of Phosphorus in Wastewater by Modified 4A Zeolite

2011 ◽  
Vol 356-360 ◽  
pp. 502-505 ◽  
Author(s):  
Yong Yin Zhang ◽  
Li Ping Wang ◽  
Er Deng Du ◽  
Yi Zhong Chen
Keyword(s):  
Reaction Time ◽  
Aluminum Chloride ◽  
Phosphorus Removal ◽  
Room Temperature ◽  
Sem Analysis ◽  
Phosphorus Concentration ◽  
Removal Mechanism ◽  
Adsorption Time ◽  
Initial Concentration ◽  
4A Zeolite

A kind of 4A zeolite, which was modified by magnesium chloride and aluminum chloride, was used to treatment phosphorus wastewater. The effect of several parameters on phosphorus removal was also investigated, including zeolite dosage, pH, phosphorus concentration and the adsorption time. The results showed that, under the conditions of pH 7, the amount of modified 4A zeolite 0.05g, reaction time 15min, room temperature, the removal efficiency of phosphorus with initial concentration 2mg/L reached 98%. The SEM analysis explained that crystalline structure of 4A zeolite has changed after modification, thus resulted in the improvement of adsorption capacity. What’s more, the phosphorus removal mechanism was also discussed.

scholarly journals Reactions of MoCl5 with 4-Methylpyridine, 2-Methylpyridine and 1-Methylimidazole in Tetrahydrofuran

2021 ◽  
Vol 37 (5) ◽  
pp. 1178-1186
Author(s):  
Rakesh Kumar ◽  
Gursharan Singh
Keyword(s):  
1H Nmr ◽  
13C Nmr ◽  
Room Temperature ◽  
Nitrogen Atmosphere ◽  
Transmission Mode ◽  
Vacuum Line ◽  
Ir Transmission ◽  
Ft Ir ◽  
Stoichiometric Ratios

MoCl5 reactions with 4-methylpyridine/2-methylpyridine/1-methylimidazole in THF in 1:1/1:2 stoichiometric ratios, at room temperature were carried out. The following products were synthesized: MoO2Cl(C6H7N), 1;Mo2O2Cl5(C6H7N)2(C4H8O)2,2; Mo4O4Cl4(C6H7N)3(C4H8O)2, 3 and Mo2O4Cl4(C4H6N)2(C4H8O), 4. These compounds have been investigated by FT-IR (transmission mode), FT-1H NMR, FT -13C NMR, microbiological, LC-MS and elemental (C, H, N, Mo, Cl) studies. In view of the sensitivity of all the reactants and products towards oxidation/hydrolysis by air/moisture, all the reactions and products were handled using dry nitrogen atmosphere in vacuum line. LC-MS and elemental studies agree with the formulae of compounds.

scholarly journals Impedimetric Detection of Ammonia and Low Molecular Weight Amines in the Gas Phase with Covalent Organic Frameworks

Sensors ◽  
2020 ◽  
Vol 20 (5) ◽  
pp. 1385 ◽  
Author(s):  
Andrés Rodríguez ◽  
Elio Rico ◽  
Cesar Sierra ◽  
Oscar Rodríguez
Keyword(s):  
Molecular Weight ◽  
Room Temperature ◽  
Nitrogen Adsorption ◽  
Low Molecular Weight ◽  
Covalent Organic Frameworks ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Nitrogen Adsorption Isotherms ◽  
Significant Interference

Two Covalent Organic Frameworks (COF), named TFP-BZ and TFP-DMBZ, were synthesized using the imine condensation between 1,3,5-triformylphloroglucinol (TFP) with benzidine (BZ) or 3,3-dimethylbenzidine (DMBZ). These materials were deposited, such as films over interdigitated electrodes (IDE), by chemical bath deposition, giving rise to TFP-BZ-IDE and TFP-DMBZ-IDE systems. The synthesized COFs powders were characterized by Powder X-Ray Diffraction (PXRD), Fourier Transform Infrared spectroscopy (FT-IR), solid-state Nuclear Magnetic Resonance (ssNMR), nitrogen adsorption isotherms, Scanning Electron Microscopy (SEM), and Raman spectroscopy, while the films were characterized by SEM and Raman. Ammonia and low molecular weight amine sensing were developed with the COF film systems using the impedance electrochemical spectroscopy (EIS). Results showed that the systems TFP-BZ-IDE and TFP-DMBZ-IDE detect low molecular weight amines selectively by impedimetric analysis. Remarkably, with no significant interference by other atmospheric gas compounds such as nitrogen, carbon dioxide, and methane. Additionally, both COF films presented a range of sensitivity at low amine concentrations below two ppm at room temperature.

scholarly journals A New Green Catalyst for Synthesis of bis-Macromonomers of Polyethylene Glycol (PEG)

2020 ◽  
Vol 14 (4) ◽  
pp. 468-473
Author(s):  
Sara Haoue ◽  
◽  
Hodhaifa Derdar ◽  
Mohammed Belbachir ◽  
Amine Harrane ◽  
...  
Keyword(s):  
Polyethylene Glycol ◽  
Reaction Time ◽  
Exchange Process ◽  
Reaction Conditions ◽  
Green Catalyst ◽  
Molecular Weights ◽  
Uv Visible ◽  
Optimal Reaction ◽  
Thermal Stability Of ◽  
End Group

A new method to synthesise polyethylene glycol dimethacrylate (PEGDM) with various molecular weights (1000, 3000, 6000 and 8000 g/mol) of polyethylene glycol (PEG) has been developed. This technique consists in using Maghnite-H+ as eco-catalyst to replace еriethylamine, which is toxic. Maghnite-H+ is a proton exchanged montmorillonite clay which is prepared through a simple exchange process. Synthesis experiments are performed in solution using dichloromethane as solvent in the presence of methacrylic anhydride. The effect of reaction time, temperature, amount of catalyst and amount of methacrylic anhydride is studied in order to find the optimal reaction conditions. The synthesis in solution leads to the best yield (98 %) at room temperature for the reaction time of 5 h. The structure of the obtained macromonomers (PEGDM) is confirmed by FTIR, 1H NMR and 13C NMR, where the methacrylate end groups are clearly visible. Thermogravimetric analysis (TGA) is used to study the thermal stability of these obtained macromonomers. The presence of unsaturated end group was confirmed by UV-Visible analysis.

A Clean, Benign, Energy Efficient One-Pot Multicomponent Synthesis and Bio-evaluation of Novel [1,2,4]Triazolo[1,5-a]quinolines

2021 ◽  
Vol 6 (2) ◽  
pp. 111-115
Author(s):  
H.P. Parekh ◽  
M.H. Chauhan ◽  
N.L. Solanki ◽  
V.H. Shah
Keyword(s):  
Room Temperature ◽  
Cost Effective ◽  
Second Step ◽  
Mass Spectral Data ◽  
Multicomponent Synthesis ◽  
One Pot ◽  
Green Catalyst ◽  
Mass Spectral ◽  
Elemental Analyses ◽  
Ft Ir

In present work, a series of novel [1,2,4]triazolo[1,5-a]quinoline derivatives (HP-101-110) have been synthesized using multi-component reaction at room temperature in the presence of ammonium chloride as mild, cost effective green catalyst along with water as eco-friendly green solvent. The synthesis of 1,2,4-triazolo[1,5-a]quinolines (HP-101-110) was achieved by two step process. In first step, diversified Hantzsch pyridine reaction of an appropriate aromatic aldehyde, malononitrile, dimedone and benz hydrazide using ethanol as a solvent gives N-(2-amino-3-cyano-7,7-dimethyl-5-oxo-4-phenyl-5,6,7,8- tetrahydro-quinolin-1(4H)-yl)-4-hydroxybenzamide derivatives. In the second step, synthesis of the final product 2-(4-hydroxyphenyl)-8,8-dimethyl-6-oxo-5-phenyl-6,7,8,9-tetrahydro[1,2,4]triazolo[1,5- a]-quinoline-4-carbonitriles was achieved by the intramolecular cyclization of step 1 product.The structure of all the synthesized compounds (HP101-110) has been elucidated by FT-IR, 1H & 13C NMR, mass spectral data and elemental analyses.

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