Preparation and Characterization of Compounds Based on Poly(hydroxymethylacrylamide) and Post-consumer Polypropylene

2016 ◽  
Vol 10 (3) ◽  
pp. 291-298 ◽  
Author(s):  
Ilma Cirne ◽  
◽  
Maria Esperidiao ◽  
Jaime Boaventura ◽  
Elizabete Lucas ◽  
...  
Keyword(s):  
Polymer Composites ◽  
Food Packaging ◽  
Low Cost ◽  
Condensation Reaction ◽  
Polymerization Reaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Swelling Capacity ◽  
Ft Ir

In this work, in order to obtain materials with potential for treatment of water from oil industry, polymer composites were synthesized by polymerization reaction via free radical using n-hydroxymethyl acrylamide (HMAA) in the presence of post-consumer polypropylene (PP) with subsequent condensation reaction catalyzed by heating, which avoids the use of crosslinking agents. The products were characterized by Fourier transform infrared spectroscopy (FT-IR), optical microscopy (OM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and X-ray diffraction (XRD). Moreover, the bulk density and the degree of swelling were also determined. The synthesis was shown to be reproducible and led to achieving polymer composites with high levels of PP after usage from food packaging, which can be associated with a relatively low cost of production. The swelling capacity and the thermal stability of the composite increased with increasing PP content in the mixture.

Liquid crystalline polyureas with oligo(ethylene glycol) sequences

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Shahram Mehdipour-Ataei ◽  
Leila Akbarian-Feizi
Keyword(s):  
Liquid Crystalline ◽  
Spectroscopic Method ◽  
Polymerization Reaction ◽  
X Ray Diffraction ◽  
Subsequent Reaction ◽  
Scanning Calorimetry ◽  
Polar Solvents ◽  
X Ray ◽  
H Nmr ◽  
Ft Ir

AbstractA diamine monomer containing ester, amide and ether functional groups was prepared and its polymerization reaction with different diisocyanates to give main chain poly(ester amide ether urea)s was investigated. The monomer was synthesized via reaction of terephthaloyl chloride with 4-hydroxybenzoic acid and subsequent reaction of the resulted diacid with 1,8-diamino-3,6-dioxaoctane. The polymers were characterized by FT-IR and 1H-NMR spectroscopic method and elemental analysis. The resulting polymers exhibited excellent solubility in polar solvents. Crystallinity of the resulted polymers was evaluated by wide-angle X-ray diffraction (WXRD) method, and they exhibited semi-crystalline patterns. The glass transition temperatures (Tg) of the polymers determined by differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) were in the range of 88-112 °C. The temperatures for 10% weight loss (T10) from their thermogravimetric analysis (TGA) curves were found to be in the range of 297-312 °C in air. Also the prepared polyureas showed liquid crystalline character.

Fabrication and characterization of smart karaya gum/sodium alginate semi-IPN microbeads for controlled release of D-penicillamine drug

2020 ◽  
pp. 096739112090447
Author(s):  
O Sreekanth Reddy ◽  
MCS Subha ◽  
T Jithendra ◽  
C Madhavi ◽  
K Chowdoji Rao
Keyword(s):  
Drug Release ◽  
Sodium Alginate ◽  
Release Kinetics ◽  
Polymerization Reaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Drug Release Kinetics ◽  
Swelling Capacity ◽  
Release Data ◽  
Karaya Gum

This article reports the fabrication of pH-sensitive microbeads from sodium alginate (SA) and modified karaya gum (KG). KG was modified by graft copolymerization using 2-hydroxyethyl methacrylate (2-HEMA) through in situ free radical polymerization reaction. The graft copolymer was blended with SA to develop microbeads by a simple ionotropic gelation technique. The microbeads were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, and scanning electron microscopy. The effect of %HEMA and polymer blend ratio on the swelling capacity was investigated. Drug release kinetics of the microbeads was investigated under both pH 7.4 and pH 1.2 at 37°C. The drug release kinetics was analyzed by evaluating the release data using different kinetic models.

Synthesis and Characterization of Zn Nanoparticles by Using Hetero-Bicyclic Compound

2014 ◽  
Vol 938 ◽  
pp. 3-8
Author(s):  
V. Pushpanathan ◽  
D. Suresh Kumar
Keyword(s):  
Condensation Reaction ◽  
Energy Dispersive Spectrum ◽  
Hydroxyl Groups ◽  
Bicyclic Compound ◽  
X Ray Diffraction ◽  
X Ray ◽  
Free Hydroxyl ◽  
Ft Ir ◽  
Esi Mass Spectrometry

The 1:1 condensation reaction between benzil and tris (hydroxymethyl) aminomethane in methanol yields a hetero bicyclic compound 5-(hydroxymethyl)-1,2-diphenyl-3,7-dioxa-8-aza-bicyclo [3.2.octan-2-ol. It was characterized by FT-IR, NMR (1H and 13C) spectroscopy and ESI mass spectrometry. The structure was conclusively determined by X-ray diffractrometric analysis. The structure shows a hetero bicyclic ring system. It consists of six membered morpholine and five membered oxazolidine rings with free hydroxyl groups. This bicyclic compound was used as a reducing and stabilizing agent to prepare zinc nanoparticles. The morphology and structure were characterized by field emission scanning electron microscope (FE-SEM), powder X-ray diffraction (XRD), and energy dispersive spectrum analysis (EDS).

Preparation and characterization of pure and copper-doped PVC films

2017 ◽  
Vol 37 (1) ◽  
pp. 83-92 ◽  
Author(s):  
K. Bhagya Sree ◽  
Y. Madhava Kumar ◽  
N.O. Gopal ◽  
Ch. Ramu
Keyword(s):  
Polymer Film ◽  
Polymer Films ◽  
Dopant Concentration ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Bending Vibrations ◽  
Paramagnetic Resonance ◽  
Solution Cast ◽  
Ft Ir

Abstract Pure and Cu2+-doped polyvinyl chloride (PVC) polymer films were prepared using the solution cast technique. Investigations were conducted using DSC, TGA, XRD, FT-IR, UV–Vis, SEM and EPR. Differential scanning calorimetry studies suggested that the Cu2+ samples have higher values of the glass transition (Tg) temperature, and thermo gravimetric studies show that weight loss of polymer film indicates the improved thermal stability of the polymer film. The features of the complexation of the polymer films were studied by X-ray diffraction. FT-IR spectra exhibits the bands in three regions, which are attributed to C–Cl, C–C and numerous CH groups of stretching and bending vibrations. The absorption spectra have been recorded in the wavelength range 200–900 nm. The absorption edge, direct bandgap, indirect bandgap and urbach energy have been evaluated. Film morphology was examined by scanning electron microscopy. XRD, DSC and SEM reveal the amorphous nature and surface morphology of polymer films, respectively. Electron paramagnetic resonance studies were used to calculate the number of spins and paramagnetic susceptibility as a function of dopant concentration, all the Cu2+-doped PVC samples exhibit signal with g values g⊥=2.176 and g||=2.254. The observed variation in the EPR signal intensity is due to variation in the dopant concentration.

scholarly journals Green anionic polymerization of vinyl acetate using Maghnite-Na+ (Algerian MMT): synthesis characterization and reactional mechanism

2021 ◽  
Vol 1 (1) ◽  
Author(s):  
Badia Imene Cherifi ◽  
Mohammed Belbachir ◽  
Abdelkader Rahmouni
Keyword(s):  
Vinyl Acetate ◽  
Polymerization Reaction ◽  
Resonance Spectroscopy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
H Nmr ◽  
Simple Filtration ◽  
Renewable Material ◽  
Ft Ir ◽  
C Nmr

AbstractIn this work, the green polymerization of vinyl acetate is carried out by a new method which consists in the use of clay called Maghnite-Na+ as an ecological catalyst, non-toxic, inexpensive and recyclable by simple filtration. X-ray diffraction (XRD) showed that Maghnite-Na+ is successfully obtained after cationic treatment (sodium) on raw Maghnite. It is an effective alternative to replace toxic catalysts such as benzoyl peroxide (BPO) and Azobisisobutyronitrile (AIBN) which are mostly used during the synthesis of polyvinyl acetate (PVAc) making the polymerization reaction less problematic for the environment. The synthesis reaction is less energetic by the use of recycled polyurethane as container for the reaction mixture and which is considered as a renewable material and a good thermal insulator which maintains the temperature at 0 °C for 6 h. The reaction in bulk is also preferred to avoid the use of a solvent and therefore to stay in the context of green chemistry. In these conditions, the structure of obtained polymer is established by Nuclear Magnetic Resonance Spectroscopy 1H NMR and 13C NMR. Infrared spectroscopy (FT-IR) is also used to confirm the structure of PVAc. Thermogravimetric analysis (TGA) showed that it is thermally stable and it starts to degrade from 330 °C while Differential Scanning calorimetry (DSC) shows that this polymer has a glass transition temperature (Tg  = 50 °C). The composition in PVAc/Maghnite-Na+ (7 wt% of catalyst) is the most tensile resistant with a force of 182 N and a maximum stress of 73.16 MPa, the most flexible (E  = 955 MPa) and the most ductile (εr  = 768%).

scholarly journals Green Polymerization of Vinyl Acetate Using Maghnite-Na+, an Exchanged Montmorillonite Clay, as an Ecologic Catalyst

2021 ◽  
Vol 15 (2) ◽  
pp. 183-190
Author(s):  
Badia Imene Cherifi ◽  
◽  
Mohammed Belbachir ◽  
Souad Bennabi ◽  
◽  
...  
Keyword(s):  
Vinyl Acetate ◽  
Polyvinyl Acetate ◽  
Polymerization Reaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Thermal Insulator ◽  
Simple Filtration ◽  
Renewable Material ◽  
Ft Ir

In this work, the green polymerization of vinyl acetate is carried out by a new method which consists in the use of clay called Maghnite-Na+ as an ecological catalyst, non-toxic, inexpensive and recyclable by a simple filtration. X-ray diffraction and scanning electron microscopy showed that Maghnite-Na+ is successfully obtained after cationic treatment (sodium) on crude maghnite. It is an effective alternative to replace toxic catalysts such as benzoyl peroxide and azobisisobutyronitrile which are mostly used during the synthesis of polyvinyl acetate (PVAc) making the polymerization reaction less problematic for the environment. The synthesis reaction is less energetic by the use of recycled polyurethane as a container for the reaction mixture and is considered as a renewable material and a good thermal insulator maintaining the temperature of 273 K for 6 h. The reaction in bulk is also preferred to avoid the use of a solvent and therefore to stay in the context of green chemistry. In these conditions, the structure of obtained polymer is established by 1H NMR and 13C NMR. Infrared spectroscopy (FT-IR) was also used to confirm the structure of PVAc. Thermogravimetric analysis showed that it is thermally stable and starts to degrade at 603 K while differential scanning calorimetry showed that this polymer has a glass transition temperature Tg of 323 K.

scholarly journals ENHANCEMENT OF GLIBENCLAMIDE DISSOLUTION RATE BY SOLID DISPERSION METHOD USING HPMC AND PVP

2019 ◽  
pp. 19-24 ◽  
Author(s):  
ARIF BUDIMAN ◽  
IYAN SOPYAN ◽  
DENIA SEPTY RIYANDI
Keyword(s):  
Dissolution Rate ◽  
Solid Dispersion ◽  
Solid Dispersions ◽  
Hydroxypropyl Methylcellulose ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Rate Test ◽  
Ft Ir

Objective: The aim of this study was to investigate the effects of changing in the proportions of the solid dispersion formula on the dissolution rate of glibenclamide. Methods: Solid dispersions were prepared by solvent evaporation method by using methanol as solvent, hydroxypropyl methylcellulose (HPMC) and polyvinyl pyrrolidone (PVP) as polymers. The prepared product was evaluated by the saturated solubility test and the dissolution rate test. The prepared product was characterized by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), and powder X-ray diffraction (PXRD) and Scanning Electron Microscopy (SEM). Results: The result showed solid dispersion with a ratio of glibenclamide: PVP: HPMC (1: 3: 6) has the highest increase in solubility (20 fold) compared to pure glibenclamide. This formula also showed an improvement in dissolution rate from 19.9±1.19% (pure glibenclamide) to 99±1.60% in 60 min. Characterization of FT-IR showed that no chemical reaction occurred in solid dispersion of glibenclamide. The results of X-ray diffraction analysis showed an amorphous form in all solid dispersion formulas. The results of DSC analysis showed that endothermic peak melting point of solid dispersion occurred, and the morphology of solid dispersion was more irregular than pure glibenclamide based on SEM characterization Conclusion: The solid dispersion of glibenclamide using PVP: HPMC as carriers can increase the solubility and dissolution rate compared to pure glibenclamide.

scholarly journals Study on the Miscibility of Polypyrrole and Polyaniline Polymer Blends

2018 ◽  
Vol 2018 ◽  
pp. 1-5 ◽  
Author(s):  
Tekalign A. Tikish ◽  
Ashok Kumar ◽  
Jung Yong Kim
Keyword(s):  
Differential Scanning Calorimetry ◽  
Polymer Blends ◽  
Processing Method ◽  
Phase Behaviour ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Amorphous Nature ◽  
Ft Ir

We report on the miscibility and phase behaviour of polypyrrole-polyaniline (PPy/PANI) as a function of blend composition. The PPy/PANI blends were prepared by solution processing method, using dimethyl sulfoxide (DMSO) solvent. Characterization of the polymer blends was carried out based on the data analysis from Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The PPy/PANI system was successfully formed blends in DMSO solvent. The polymer blends showed almost amorphous nature in XRD spectra because of intermolecular interaction between PPy and PANI macromolecules, which was confirmed by FT-IR data. Specifically, the DSC result for the PPY : PANI = 50 : 50 wt.% blend showed only one glass transition temperature (Tg), which indicates that the two polymers are well miscible without undergoing any phase separation.

scholarly journals Preparation and Characterization of Cetyl Trimethylammonium Intercalated Sericite

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Hao Ding ◽  
Yuebo Wang ◽  
Yu Liang ◽  
Faxiang Qin
Keyword(s):  
Ion Exchange ◽  
Interlayer Space ◽  
Xrd Analysis ◽  
Acid Activation ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Intercalated sericite was prepared by intercalation of cetyl trimethylammonium bromide (CTAB) into activated sericite through ion exchange with the following two steps: the activation of sericite by thermal modification, acid activation and sodium modification; the ion exchange intercalation of CTA+into activated sericite. Effects of reaction time, reaction temperature, CTAB quantity, kinds of medium, and aqueous pH on the intercalation of activated sericite were examined by X-ray diffraction (XRD) analysis, Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The results indicated that the CTA+entered sericite interlayers and anchored in the aluminosilicate interlayers through strong electrostatic attraction. The arrangement of CTA+in sericite interlayers was that alkyl chain of CTA+mainly tilted at an angle about 60° (paraffin-type bilayer) and 38° (paraffin-type monolayer) with aluminosilicate layers. The largest interlayer space was enlarged from 0.9 nm to 5.2 nm. The intercalated sericite could be used as an excellent layer silicate to prepare clay-polymer nanocomposites.

scholarly journals A Novel Green Synthesis Method of Poly (3-Glycidoxypropyltrimethoxysilane) Catalyzed by Treated Bentonite

2020 ◽  
Vol 15 (2) ◽  
pp. 290-303
Author(s):  
Nadia Embarek ◽  
Nabahat Sahli
Keyword(s):  
Ring Opening ◽  
Low Cost ◽  
Synthesis Method ◽  
Bulk Polymerization ◽  
Scanning Calorimetry ◽  
Epoxy Ring ◽  
Polymer Yield ◽  
Epoxy Ring Opening ◽  
Ft Ir

The present work focuses on the preparation and characterization of poly(3-Glycidoxypropyltrimethoxysilane) (PGPTMS) under mild conditions. Ring-opening polymerization of the 3-Glycidoxypropyltrimethoxysilane (GPTMS) is initiated with the bentonite of Maghnite-H+ (Mag-H+), an ecologic and low-cost catalyst. The evolution of epoxy ring-opening was studied in bulk and in solution using CH2Cl2 as solvent, as well as the influences of several factors such as the amount of Mag-H+, polymerization time and temperature on the yield of polymer were investigated. The best polymer yield (30 %) was obtained in bulk polymerization at room temperature (20 °C) for a reaction time 8 h, and it’s increases with time and reaches 68 % for 7 days. The structures of the obtained polymers (PGPTMS) were confirmed respectively by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR). The thermal properties of the prepared polymers were given by Differential Scanning Calorimetry (DSC) and thermogravimetric analysis (TGA), the Tg of PGPTMS is recorded at -31.27 °C, and it is thermally stable with a degradation start temperature greater than 300 °C, all  decomposition stopped at 600 °C. Copyright © 2020 BCREC Group. All rights reserved

Sign in / Sign up

Export Citation Format

Share Document